Label: RETINOL COLLAGEN lotion
- NDC Code(s): 83872-029-01
- Packager: Shenzhen XiaoMai Manufacturing Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 3, 2024
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Active ingredients
Palmitoyl Tetrapeptide-7-2%
Chamomilla Recutita (Matricaria) Flower Extract-5%
Palmitoyl Oligopeptide-5%
Ascorbic Acid-5%
Tocopherol-1%
Snail Secretion Filtrate-1%
Panthenol-1%
Punica Granatum Extract-1%
Euterpe Oleracea Fruit Oil-1%
Theobroma Grandiflorum Seed Butter-0.5%
Daucus Carota Sativa (Carrot) Seed Oil-0.5 - Purpose
- Uses
- Warnings
- Do not use
- When using this product
- WHEN USING SECTION
- Keep out of reach of children
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Directions
Indications:
IMPROVE SKIN QUALITY AND REDUCE WRINKLES AND FINE LINES.
PROMOTE A YOUTHFUL APPEARANCE AND EVEN SKIN TONE.
REDUCE DARK SPOTS, PIGMENTATION, AND UNEVEN SKIN TONE.Uses:
Twice daily, in the morning and evening. Recommended usage amount: A pea to cherry-sized amount (about 2-3 grams) is sufficient for each use. - Inactive ingredients
- Other information
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RETINOL COLLAGEN
retinol collagen lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83872-029 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID 2 mg in 100 g PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL 2 mg in 100 g THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM) (THEOBROMA GRANDIFLORUM SEED BUTTER - UNII:I711F13FXM) THEOBROMA GRANDIFLORUM SEED BUTTER 0.5 mg in 100 g PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) (PALMITOYL TETRAPEPTIDE-7 - UNII:Q41S464P1R) PALMITOYL TETRAPEPTIDE-7 2 mg in 100 g TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8) TOCOPHEROL 1 mg in 100 g Inactive Ingredients Ingredient Name Strength SYNTHETIC BEESWAX (UNII: 08MNR5YE2R) 1 mg in 100 g BENZYL SALICYLATE (UNII: WAO5MNK9TU) 1 mg in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83872-029-01 50 g in 1 BOTTLE; Type 0: Not a Combination Product 03/04/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 03/04/2024 Labeler - Shenzhen XiaoMai Manufacturing Co., Ltd. (712999147) Establishment Name Address ID/FEI Business Operations Shenzhen XiaoMai Manufacturing Co., Ltd. 712999147 manufacture(83872-029)