Label: AAPE CONTINUOUS RENEWAL SERUM- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 62041-210-01, 62041-210-02 - Packager: PROSTEMICS Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated August 26, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Water, Human Adipocyte Conditioned Media Extract, Butylene Glycol, Glycerin, PEG/PPG-17/6 Copolymer, Bis-PEG-18, Methyl Ether Dimethyl Silane, PEG-60 Hydrogenated Castor Oil, Caprylyl Glycol, Carbomer, Tromethamine, Phenyl Trimethicone, Ethylhexylglycerin, Glyceryl, Citrate/Lactate/Linoleate/Oleate, Biosaccharide Gum-1, Trehalose, 1,2-Hexanediol, Olea Europaea (Olive) Fruit Oil, Polysorbate 60, Betula Platyphylla, Japonica Juice, Portulaca Oleracea Extract, Sodium Hyaluronate, Xanthan Gum, Rubus Idaeus (Raspberry) Fruit Extract, Gentiana Lutea Root Extract, Achillea Millefolium Extract, Artemisia Absinthium Extract, Arnica Montana Flower Extract, Beta-Glucan, Hydrolyzed Extensin, Acetyl Hexapeptide-8, PEG-40 Hydrogenated, Castor Oil, PPG-26-Buteth-26, Copper Tripeptide-1 - PURPOSE
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WARNINGS
Warnings:
For external use only
1. Discontinue use if signs of irritation or rashes appear. If symptoms get worse, consult with a dermatologist. 1) In case of swelling, itching, or other side effects while or after using this product
2. Do not apply to open wounds.
3. Avoid contact with eyes.
Storage and handling
4. Replace the cap after use
5. Keep out of reach of children.
6. Avoid direct sunlight. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AAPE CONTINUOUS RENEWAL SERUM
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62041-210 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.80 g in 40 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.01 g in 40 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62041-210-02 1 in 1 CARTON 08/01/2019 1 NDC:62041-210-01 40 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/01/2019 Labeler - PROSTEMICS Co., Ltd. (689605919) Registrant - PROSTEMICS Co., Ltd. (689605919) Establishment Name Address ID/FEI Business Operations Prostemics Co., Ltd. Factory 695687674 manufacture(62041-210)
