Label: RETINOL CREAM FOR FACE MOISTURIZER FACE CREAM cream
- NDC Code(s): 84732-081-01
- Packager: Dongguan Haiyi Technology Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 3, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
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Inactive ingredient
Aqua, Collagen, Organic Sunflower Oil, Palm Oil,Polysorbate 20, Potassium Phosphate, Shea Butter, Vitamin E, OrganicAloe Vera, Cassia Angustifolia Seed (Hyaluronic Acid 5% KosherVegetable Glycerine, (Organic Jojoba oil, Camellia Sinensis (Tea) Extract,Panthenol (Vitamin B5),Xanthan Gum, Citric Acid, Phospholipids,Pentylene Glycol, Stearic Acid, Glycerin Stearate, Phenoxyethanol,Ethyhexyl Glycerin.
- Purpose section
- Warning
- stop use
- not use
- OUT OF CHILDREN
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HOW TO USE
- Cleanse and Tone: Start with clean skin, using a cleanser and toner suited to your skin type.
- Use a Pea-Sized Amount: Scoop a small amount of cream (about a pea-sized amount) and warm it between your fingers to help with absorption.
- Apply Gently: Dot the cream onto your forehead, cheeks, nose, and chin. Spread it evenly using gentle, upward and outward motions. Avoid the eye area unless the cream is specifically formulated for it.
- Massage In: Lightly massage the cream into the skin for better absorption and circulation.
- Wait Before Layering: Allow a few minutes for the cream to absorb before applying any other products, such as makeup or sunscreen.
- Dosage
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RETINOL CREAM FOR FACE MOISTURIZER FACE CREAM
retinol cream for face moisturizer face cream creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84732-081 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength RETINOL (UNII: G2SH0XKK91) (RETINOL - UNII:G2SH0XKK91) RETINOL 1 mg in 50 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) CASSIA ANGUSTIFOLIA SEED EXTRACT (UNII: UC1K4NA7ML) WATER (UNII: 059QF0KO0R) EQUINE COLLAGEN (UNII: 3221SCV0LS) SHEA BUTTER (UNII: K49155WL9Y) POLYSORBATE 20 (UNII: 7T1F30V5YH) VITAMIN E POLYETHYLENE GLYCOL SUCCINATE (UNII: O03S90U1F2) SUNFLOWER OIL (UNII: 3W1JG795YI) POTASSIUM PHOSPHATE (UNII: B7862WZ632) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84732-081-01 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/04/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 11/04/2024 Labeler - Dongguan Haiyi Technology Co.,Ltd. (722030807) Establishment Name Address ID/FEI Business Operations Dongguan Haiyi Technology Co.,Ltd. 722030807 manufacture(84732-081)