Label: ANTI WRINKLE EYE CREAM cream
- NDC Code(s): 84117-009-01, 84117-009-02
- Packager: Shenzhen Hengkaifeng Commerce and Trade Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 11, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Purpose
- Use
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Warnings
Keep out of reach of children. For external use only. Before using,test for sensitivity
on a small area of skin.Do not use on damaged skin. Use only as directed. Avoid
contact with eyes.Rinse with warm water to remove. Stop use and consult your
physician it rash occurs. Do not ingest. lf swallowed, get medical help or contact
a Poison Control Center right away! Do not use if safety seal is breken or missing.
Store in a cool, dry place. - Keep Out Of Reach Of Children
- Directions Of Safe Use:
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Inactive ingredients
Water, Caprylic/Capric Triglyceride, Glycerin, Butylene Glycol, Pentaerythrityl
Distearate, Shea Butter Ethyl Esters, Cetearyl Olivate, Phenoxyethanol, Benzyl
Alcohol, Sorbitan Olivate, Sodium Hydroxide, Sodium Hyaluronate, Sodium
Stearoyl Glutamate, Copernicia Cerifera Cera, Propanediol, Glycogen, Sodium
Gluconate, Caffeine ,Ascorbic Acid ,Hyaluronic acid,Polysorbate 20,
Dimethylaminoethanol, Ethylhexylglycerin, Dehydroacetic Acid, Citric Acid,
Helianthus Annuus Seed Oil, 1,2-Hexanediol, Caprylyl Glycol, Tocopherol,
Xanthan Gum, Ethyl Ferulate, Humulus Lupulus Extract. - DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTI WRINKLE EYE CREAM
anti wrinkle eye cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84117-009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RETINOL (UNII: G2SH0XKK91) (RETINOL - UNII:G2SH0XKK91) RETINOL 1 g in 100 g Inactive Ingredients Ingredient Name Strength ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SUNFLOWER OIL (UNII: 3W1JG795YI) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) TOCOPHEROL (UNII: R0ZB2556P8) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CETEARYL OLIVATE (UNII: 58B69Q84JO) PHENOXYETHANOL (UNII: HIE492ZZ3T) HYALURONIC ACID (UNII: S270N0TRQY) DEHYDROACETIC ACID (UNII: 2KAG279R6R) XANTHAN GUM (UNII: TTV12P4NEE) PROPANEDIOL (UNII: 5965N8W85T) WATER (UNII: 059QF0KO0R) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CAFFEINE (UNII: 3G6A5W338E) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ETHYL FERULATE (UNII: 5B8915UELW) BENZYL ALCOHOL (UNII: LKG8494WBH) ASCORBIC ACID (UNII: PQ6CK8PD0R) POLYSORBATE 20 (UNII: 7T1F30V5YH) PENTAERYTHRITYL DISTEARATE (UNII: 697WOT8HNB) SHEA BUTTER ETHYL ESTERS (UNII: V2CI786FPG) CAPRYLYL GLYCOL (UNII: 00YIU5438U) HOPS (UNII: 01G73H6H83) SODIUM GLUCONATE (UNII: R6Q3791S76) SORBITAN OLIVATE (UNII: MDL271E3GR) PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A) GLYCERIN (UNII: PDC6A3C0OX) SODIUM HYDROXIDE (UNII: 55X04QC32I) DEANOL (UNII: 2N6K9DRA24) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) GLYCOGEN (UNII: 309GSC92U1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84117-009-01 50 g in 1 CANISTER; Type 0: Not a Combination Product 05/11/2024 2 NDC:84117-009-02 30 g in 1 CANISTER; Type 0: Not a Combination Product 05/11/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 05/11/2024 Labeler - Shenzhen Hengkaifeng Commerce and Trade Co., Ltd (444722774) Establishment Name Address ID/FEI Business Operations Shenzhen Hengkaifeng Commerce and Trade Co., Ltd 444722774 manufacture(84117-009) , label(84117-009)