Vitamin E
Vitamin E detail image 2
Vitamin E detail image 3
ANTIOXIDANTS & STABILIZERS / RAW MATERIALSCustomizableSamples available

Product overview

For antioxidants and vitamins, the ingredient catalog includes the raw-material entry for Vitamin E.

What role does Vitamin E play in a cosmetic formula?

Vitamin E appears in the Antioxidants & Stabilizers group for antioxidants and vitamins, while the final formula and material grade determine its finished-product role.

How can a formulator test Vitamin E before scale-up?

To assess Vitamin E for antioxidants and vitamins, review a small sample in the intended formula and record dispersion and compatibility against the selected grade documents.

What determines the suitable use level of Vitamin E?

The listing for Vitamin E does not set a universal use level; select one only from the chosen grade documentation and a review of the complete antioxidants and vitamins formula.

Formula customization
Sample review first
Quality check before dispatch
Batch documents on request
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Formula overview

Face and personal care

Product Highlights

  • Antioxidants & Stabilizers · Face and personal care
  • Stability and skin-support ingredient
  • Actives cover listed active, humectant, emollient, butter
  • 5 documented key materials on this SKU
  • Samples available (Laboratory sample available on request)

Key ingredients

  • Glycerin: 4%

  • Squalane: 3%

  • Butyrospermum Parkii Butter: 4%

  • Panthenol: 2%

  • Vitamin E

Percentages are the guide levels recorded for this SKU. They describe composition, not a drug effect or a batch assay.

Attributes

  • Cosmetic grade
  • Formula-ready
  • Customizable use level
  • Function-led ingredient
  • Cruelty-free
  • Suitable for brand formulas
  • Chassis compatible
  • Clear cosmetic role

Key ingredients

Key Ingredients & Their Benefits

Vitamin E lists the recorded identity of the named material below. Typical % values are formulation guides for a finished chassis that uses this material — not confirmed batch assays for this raw-material SKU.

Formula reference — key actives

IngredientPrimary FunctionKey BenefitsCompliance & Market ProofTypical %
Vitamin ECosmetic ingredient named on this SKUVitamin E is named from the product record. Use level and grade follow the supplier TDS.—TDS
GlycerinHumectantGlycerin in the water phase acts as a humectant to retain water in the water-based part of the system.—4%
SqualaneLight plant-derived emollientSqualane in this guide adds slip and the guide does not use mineral oil.—3%
Butyrospermum Parkii ButterShea butterRefined shea is the cushion butter. Refined grade stays paler than crude shea.—4%
PanthenolHumectant / soothingPro-vitamin B5 softens feel and supports comfort in leave-on and rinse-off guides.—2%

For a raw-material SKU, the first row is the material identity and the other rows are finished-formula partners formulators often specify with it. They are not the composition of the raw drum. Typical % is a formulation guide for vitamin-e, not a batch assay or a COA. Water is the balance of water-based chassis. Texture family: cream. No fragrance oil is built in; scent stays a buyer option. Cosmetic claims only. Run challenge, stability and pack tests on the confirmed batch. Do not use this guide as a drug, whitening, acne, antiperspirant, sunscreen, or hair-growth claim.

Full INCI ingredient list

View ingredient names in one place

Aqua (Water), Vitamin E, Glycerin, Squalane, Butyrospermum Parkii Butter, Panthenol, Ethylhexylglycerin, Sodium Benzoate, Potassium Sorbate, Citric Acid.

Ingredient encyclopedia — customization details

Deep-dive notes for the lead actives in this chassis: identity, use levels, regulatory framing, safety language, and stability/packaging guidance for professional development.

Vitamin E

Cosmetic ingredient named on this SKU

1. INCI & CAS

INCI: Vitamin E · CAS: pending supplier / regulatory confirmation for the selected grade

2. Role in the formula

Vitamin E is carried as a named cosmetic ingredient for this SKU. Identity, assay and impurities are confirmed on the supplier TDS and COA. This page does not invent a CAS or a drug effect.

3. Typical use levels (formulation guide)

  • Set the use level from the supplier TDS for the finished formula.

Refer to the supplier TDS for solvent, temperature and pH.

4. Regulatory sources & global compliance

  • Database information on Vitamin E does not replace review of the supplied grade and finished product under market rules.
  • The finished-product provisions of Regulation (EC) No 1223/2009 require a safety assessment of the finished cosmetic containing Vitamin E in the final product context.
  • Compare the received Vitamin E material with its supplier specification and review destination-market filing needs.

5. Safety & risk assessment

Use the stated level as reference guidance for cosmetic formulation; it should not be read as a drug authorization or OTC listing with patch response and finished-product stability still to be verified.

6. Stability & packaging

Keep the bulk container closed and shaded in a cool area; evaluate packaging against the formula's susceptibility to oxidation; then verify formula stability and pack compatibility on the confirmed batch.

7. Claims language (Do / Don’t)

  • Names Vitamin E as a cosmetic ingredient on this SKU
  • The development record does not demonstrate a drug effect, a clinical cure, or certification status not established for the SKU.
  • The ingredient record for Vitamin E provides no basis for skin whitening, acne treatment, antiperspirant use, sun protection, or hair growth.

Glycerin

Humectant

1. INCI & CAS

INCI: Glycerin · CAS: 56-81-5

2. Role in the formula

Glycerin serves as the polyol humectant in these cosmetic formats, while the stated percentage remains a formulation reference.

3. Typical use levels (formulation guide)

  • The level shown for gels and serums is 3–8%.
  • For creams, the reference gives 2–5% in this reference.
  • For rinse-off, the reference gives 2–4%.

The water phase is the addition point for Glycerin; a separate melt is unnecessary.

4. Regulatory sources & global compliance

  • CosIng may identify Glycerin as an ingredient, but its entry does not approve a material grade or finished formula.
  • EU cosmetics rules under Regulation (EC) No 1223/2009 require the complete cosmetic containing Glycerin to receive its own safety assessment in the final product context.
  • Verify the purchased Glycerin grade using supplier data, alongside the applicable filing rules for the destination market.

5. Safety & risk assessment

Read the recorded level as a cosmetic formulation guide; no drug approval or OTC status is conferred by this entry and the final formula should undergo patch and stability assessment.

6. Stability & packaging

Keep the bulk container closed and shaded in a cool area; where appropriate, assess an airless or pump pack for oxidation-sensitive systems; then verify formula stability and pack compatibility on the confirmed batch.

7. Claims language (Do / Don’t)

  • For cosmetic use, this entry records Glycerin in a direction centered on humectant function.
  • The available ingredient details does not demonstrate therapeutic effects, curative outcomes, or unsupported certification statements.
  • The formulation record for Glycerin provides no basis for a whitening result, acne-treatment effect, antiperspirant use, sunscreen performance, or hair growth.

Squalane

Light plant-derived emollient

1. INCI & CAS

INCI: Squalane · CAS: 111-01-3

2. Role in the formula

The guide uses plant-derived squalane, a stable hydrocarbon emollient, and does not specify mineral oil.

3. Typical use levels (formulation guide)

  • For gel-creams, use 2–6% as a formulation guide.
  • Dry oils: 10–30% for the formula.
  • The guide range for balms is 5–15% as a formulation guide.

Use the oil phase to introduce Squalane; a high-shear wax stage is not specified.

4. Regulatory sources & global compliance

  • CosIng information about Squalane does not itself authorize a particular grade or finished cosmetic.
  • Regulation (EC) No 1223/2009 sets the requirement for a safety assessment covering the complete formulation with Squalane for the product in its final form.
  • Verify the purchased Squalane grade using supplier data, alongside the applicable filing rules for the destination market.

5. Safety & risk assessment

This formulation note gives a cosmetic-use reference level; it should not be read as a drug authorization or OTC listing so assess patch response and stability in the final formula.

6. Stability & packaging

Store the bulk in a closed container in a cool, shaded place; if the formula is oxidation-sensitive, an airless or pump format may be considered; verify the chosen pack against the tested formula.

7. Claims language (Do / Don’t)

  • For cosmetic use, this entry records Squalane in a direction centered on a light-emollient role.
  • The available ingredient details does not substantiate therapeutic results, cure claims, or unverified certification claims.
  • The Squalane entry does not confirm a skin-lightening result, acne treatment, antiperspirant action, sunscreen efficacy, or hair growth.
  • EU CosIng · formulation guide, not a batch COA

Stability & QA protocol for the finished chassis

These checks are the professional release path for a finished leave-on chassis that uses this material. They describe what we verify before commercial fill — they are not published batch results for this raw-material SKU.

  • Accelerated & real-time stabilityTrack appearance, odour, pH and viscosity at agreed temperatures for the target fill and pack.
  • Freeze–thaw / thermal cyclingConfirm no phase split, precipitation or irreversible darkening after cycling.
  • Preservation challengeValidate the preservative system against the selected formula and packaging before scale-up.
  • Light / packaging compatibilityPrefer opaque or UV-protective packs where actives need light protection; check leachables and pump/dropper fit.
  • pH window controlHold the finished chassis near pH 5.0–6.0 unless the approved brief states otherwise.
  • Document gateRelease only after TDS/SDS, specification and batch COA identity are approved for the chosen material grade.
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Certified Quality & Safety Assurance

Under strict ISO 22716 GMP and U.S. FDA Cosmetic GMP site records from SGS (CN21/31217, CN21/31218), batch release and document packs support export buyers when production records exist.

  • SGS Certified
  • GMP good manufacturing practice markGMP Certified
  • ISO quality system markISO Quality
  • ISO 22716 GMP
  • US FDA COSMETIC GMP
  • SGS ISO 22716 Cosmetic GMP

    CN21/31217 · Valid to 17 Jul 2027 · Holder: Guangzhou Yuanxu Pharmaceutical

  • SGS US FDA Cosmetic GMP

    CN21/31218 · Valid to 17 Jul 2027 · Holder: Guangzhou Yuanxu Pharmaceutical

  • Foreign Trade Operator Registration

    Official company filing · China

  • UK Distributor Letter of Authorization

    Distributor authorization · United Kingdom

  • Vietnam Import and Distribution Letter of Authorization

    Import and distribution · Vietnam

  • Free Sale Certificate Authentication

    CCPIT certificate · 2024

  • Product Test Report

    SQTT laboratory · CMA accredited

  • Transport Identification Report

    Non-restricted goods by sea · CNAS

  • Safety Data Sheet

    SDS · Version 6.4

Certificate holder for the manufacturing site: Guangzhou Yuanxu Pharmaceutical Co., Ltd. Guangzhou Prink International Cosmetics Co., Ltd. uses this site; the two companies remain separately registered and are not merged. Check status in the SGS Certified Client Directory

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