Label: AAPE NUTRIENT FACIAL TONER- niacinamide liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 62041-200-01, 62041-200-02 - 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 22, 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, Butylene Glycol, PEG/PPG-17/6 Copolymer, Trehalose, Human Adipocyte Conditioned Media Extract, 1,2-Hexanediol, Caprylyl Glycol, Bis-PEG-18 Methyl Ether Dimethyl Silane, Ethylhexylglycerin, Salix Alba (Willow) Bark Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, Glycerin, Cellulose Gum, Panthenol, PEG-60 Hydrogenated Castor Oil, Hamamelis Virginiana (Witch Hazel) Leaf Water, Disodium EDTA, Glyceryl Citrate/Lactate/Linoleate/Oleate, Sodium Hyaluronate, Olea Europaea (Olive) Fruit Oil, Polysorbate 60, Lilium Candidum, Flower Extract, Leontopodium Alpinum Flower/Leaf Extract, Convallaria Majalis Bulb/Root Extract, Magnolia Liliflora Flower Extract, Paeonia Lactiflora Extract, Palmitoyl Tripeptide-5, Fragrance - 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 NUTRIENT FACIAL TONER
niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62041-200 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 2.60 g in 130 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:62041-200-02 1 in 1 CARTON 08/01/2019 1 NDC:62041-200-01 130 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(62041-200)
