Label: BIBILIP ALOE CICA DUAL MOISTURIZER- niacinamide, adenosine liquid
- NDC Code(s): 71080-0015-1, 71080-0015-2
- Packager: GTG Wellness Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 25, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients:
Water, Diisostearyl Malate, Beeswax, 1,2-Hexanediol, Cetyl Alcohol, Butyrospermum Parkii (Shea) Butter, Glyceryl Stearate, Squalane, Panthenol, Caprylic/Capric Triglyceride, Pantolactone, Madecassoside, Butylene Glycol, Dipotassium Glycyrrhizate, Hydroxypropyl Bispalmitamide MEA, Aloe Barbadensis Leaf Extract, Althaea Rosea Root Extract, Ficus Carica (Fig) Fruit Extract, Punica Granatum Fruit Extract, Morus Alba Fruit Extract, Ginkgo Biloba Nut Extract, Ammonium Acryloyldimethyltaurate/VP Copolymer,
PEG-100 Stearate, Hydrolyzed Hyaluronic Acid, Aloe Barbadensis Leaf Juice Powder, Fragrance - PURPOSE
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WARNINGS
Warnings:
1. In case of using cosmetics or after use, please consult a specialist if there is any abnormal symptom or side effect such as red spot, swelling or itching in direct sunlight.
2. Do not use on wounded areas.
3. Precautions for storage and handling
a) Keep out of reach of children.
b) Avoid direct sunlight. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BIBILIP ALOE CICA DUAL MOISTURIZER
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71080-0015 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.16 g in 8 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.003 g in 8 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Diisostearyl Malate (UNII: QBS8A3XZGQ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71080-0015-2 1 in 1 CARTON 04/01/2020 1 NDC:71080-0015-1 8 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 04/01/2020 Labeler - GTG Wellness Co., Ltd. (689458057) Registrant - GTG Wellness Co., Ltd. (689458057) Establishment Name Address ID/FEI Business Operations YUYU LnP Inc 694752447 manufacture(71080-0015)