Velvet Foot Gel
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SOFTENING / READY TO LABELCustomizableSamples available

Velvet Foot Gel

Product overview

Velvet Foot Gel is listed as a gel product for hand and foot softening, with Hydroxyethylcellulose and Propanediol on its key-ingredient list.

Who is Velvet Foot Gel intended for?

The SKU record describes Velvet Foot Gel as a gel for hand and foot softening and includes Hydroxyethylcellulose, Propanediol, and Panthenol among its key ingredients; finished results depend on the complete formula and individual conditions.

How should users apply Velvet Foot Gel?

For Velvet Foot Gel, assess appearance, texture, application feel and stability in the intended hand and foot softening application and check that the sample and selected pack match the current product documents.

What should a brand verify before launching Velvet Foot Gel?

Before release, reconcile the listed gel format and hand and foot softening application for Velvet Foot Gel with the final product specification and label.

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

Softening product line development

Product Highlights

  • Softening · Softening product line development
  • Gel finished retail-ready cosmetic for private-label fill
  • Approved base formula with packaging and label configuration reviewed against the brief
  • Actives cover humectant, humectant solvent, gum, soothing humectant
  • 4 documented key materials on this SKU
  • Samples available (1 sample pack)

Key ingredients

  • Glycerin: 5%

  • Propanediol: 3%

  • Hydroxyethylcellulose: 0.4%

  • Panthenol: 2%

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

Attributes

  • Private-label ready
  • Fill-ready formula
  • Customizable scent and shade
  • Vegan
  • Cruelty-free
  • Paraben-free
  • Phthalate-free
  • Shelf ready for brands and spas

Key ingredients

Key Ingredients & Their Benefits

Velvet Foot Gel lists the recorded key actives for this ready product below. Typical % values describe the intended chassis and are not confirmed batch assays.

Formula reference — key actives

IngredientPrimary FunctionKey BenefitsCompliance & Market ProofTypical %
GlycerinHumectantThis guide's glycerin supports moisture retention as part of the aqueous phase.—5%
PropanediolPropanediolPropanediol serves as a secondary humectant and as a solvent for some actives; it is not propylene glycol.—3%
HydroxyethylcelluloseHECHydroxyethylcellulose is the nonionic thickener for clear gels.—0.4%
PanthenolHumectant / soothingPro-vitamin B5 softens feel and supports comfort in leave-on and rinse-off guides.—2%

Typical % is a formulation guide for velvet-foot-gel, not a batch assay or a COA. Water is the balance of water-based chassis. Texture family: gel. 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), Glycerin, Propanediol, Hydroxyethylcellulose, 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.

Glycerin

Humectant

1. INCI & CAS

INCI: Glycerin · CAS: 56-81-5

2. Role in the formula

Glycerin fills a polyol-humectant role in the listed cosmetic formats. Read its percentage as formulation guidance, not an assay.

3. Typical use levels (formulation guide)

  • Gels and serums: 3–8% in this reference.
  • Creams: 2–5% for the formula.
  • The rinse-off use-level reference is 2–4%.

Use the water phase to introduce Glycerin; no melting stage is required.

4. Regulatory sources & global compliance

  • Treat any CosIng entry for Glycerin as a reference only; verify the grade and intended use under current market rules.
  • EU market placement under Regulation (EC) No 1223/2009 requires the final cosmetic with Glycerin to undergo a safety assessment before the cosmetic is placed on the EU market.
  • Compare the received Glycerin material with its supplier specification and review destination-market filing needs.

5. Safety & risk assessment

This level is a cosmetic-formulation guide; the listed level does not itself confer drug or OTC status and the final formula should undergo patch and stability assessment.

6. Stability & packaging

Maintain cool, closed, light-protected storage for the bulk material; consider an airless or pump format when oxidation sensitivity warrants it; confirm compatibility and stability using the selected formula and pack.

7. Claims language (Do / Don’t)

  • This guide frames Glycerin's cosmetic direction around humectant function.
  • This product entry does not establish medical outcomes, cure language, or a product certification not supported by the available facts.
  • The formulation record for Glycerin does not substantiate a whitening effect, acne treatment, perspiration control, sun protection, or hair growth.

Propanediol

Propanediol

1. INCI & CAS

INCI: Propanediol · CAS: 504-63-2

2. Role in the formula

1,3-propanediol serves as a cosmetic humectant and solvent in this guidance, distinct from propylene glycol.

3. Typical use levels (formulation guide)

  • The formulation record indicates 2–8% for most water chassis in this reference.

The water phase is the addition point for Propanediol.

4. Regulatory sources & global compliance

  • Treat any CosIng entry for Propanediol as a reference only; verify the grade and intended use under current market rules.
  • For an EU-market product, Regulation (EC) No 1223/2009 requires a safety assessment of the finished cosmetic containing Propanediol for the specific product as it will be marketed.
  • Use current supplier documentation for the purchased Propanediol grade and verify applicable destination-market filings.

5. Safety & risk assessment

This level is a cosmetic-formulation guide; no drug approval or OTC status is conferred by this entry while finished-product patch and stability testing remain necessary.

6. Stability & packaging

Maintain cool, closed, light-protected storage for the bulk material; if the formula is oxidation-sensitive, an airless or pump format may be considered; check the finished formula and its packaging together.

7. Claims language (Do / Don’t)

  • The listed cosmetic direction for Propanediol emphasizes propanediol solvent.
  • The ingredient record is not evidence of a drug effect, a clinical cure, or certification status not established for the SKU.
  • This guide to Propanediol cannot establish whitening, treatment of acne, perspiration control, sun protection, or hair growth.

Hydroxyethylcellulose

HEC

1. INCI & CAS

INCI: Hydroxyethylcellulose · CAS: 9004-62-0

2. Role in the formula

HEC builds clear gels without a carbomer neutralization story.

3. Typical use levels (formulation guide)

  • The stated reference for gels is 0.3–0.8% for the formula.

Disperse in glycerin or water and hydrate fully.

4. Regulatory sources & global compliance

  • A CosIng listing for Hydroxyethylcellulose provides ingredient information, not approval of a supplied grade or finished product.
  • Before EU placement, Regulation (EC) No 1223/2009 requires an assessment of the safety of the final cosmetic containing Hydroxyethylcellulose as a finished-product assessment.
  • Review the documentation for the actual Hydroxyethylcellulose grade and the filing requirements for the target market.

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 and the completed cosmetic needs its own patch and stability checks.

6. Stability & packaging

Store sealed bulk away from heat and sunlight; if the formula is oxidation-sensitive, an airless or pump format may be considered; check the finished batch's stability and package compatibility.

7. Claims language (Do / Don’t)

  • The recorded cosmetic positioning for Hydroxyethylcellulose highlights clear-gel thickener.
  • This product entry does not support drug-treatment outcomes, clinical cures, or certifications not documented for the SKU.
  • The cosmetic guidance for Hydroxyethylcellulose provides no basis for skin whitening, treatment of acne, sweat control, UV protection, or hair-growth results.
  • EU CosIng · formulation guide, not a batch COA

Stability & QA protocol for the finished chassis

These checks are the professional release path for Velvet Foot Gel. They describe what we verify before commercial fill — they are not published batch results for this ready product.

  • 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 confirmed ready product.
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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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