Label: BIBILIP HONEY COCO TOTAL CARE- niacinamide, adenosine liquid
- NDC Code(s): 71080-0016-1, 71080-0016-2
- Packager: GTG Wellness 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 May 25, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive ingredients:
Water, Glycerin, Beeswax, Cetearyl Alcohol, 1,2-Hexanediol, Butylene Glycol, Hydrogenated Vegetable Oil, Centella Asiatica Leaf Water, Honey Extract, Propolis Extract, Royal Jelly Extract, Cocos Nucifera (Coconut) Oil, Hydrogenated Coconut Oil, Butyrospermum Parkii (Shea) Butter, Stearic Acid, Diisostearyl Malate, Lavandula Angustifolia (Lavender) Extract, Rosmarinus Officinalis (Rosemary) Extract, Thymus Vulgaris (Thyme) Extract, Origanum Vulgare Flower/Leaf/Stem Extract, Dipotassium Glycyrrhizate, Madecassoside, Behenyl Alcohol, Cetearyl Glucoside, Ammonium Acryloyldimethyltaurate/VP Copolymer, Glucose, Fragrance, Glycine, Serine, Glutamic Acid, Aspartic Acid, Leucine, Alanine, Lysine, Arginine, Tyrosine, Phenylalanine, Valine, Threonine, Proline, Isoleucine, Histidine, Methionine, Cysteine
- PURPOSE
-
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
-
INGREDIENTS AND APPEARANCE
BIBILIP HONEY COCO TOTAL CARE
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71080-0016 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) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71080-0016-2 1 in 1 CARTON 04/01/2020 1 NDC:71080-0016-1 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(71080-0016)
