Label: PAHABA SOLUTION- niacinamide liquid
- NDC Code(s): 81715-0004-1
- Packager: JH Science 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 April 4, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Aqua, Glycerin, Dipropylene Glycol, Niacinamide, Glycolic Acid, 1,2-Hexanediol,Gluconolactone, Potassium Hydroxide, Xanthan Gum, Panthenol, Salicylic Acid, Hydroxye, thylcellulose, Ammonium Acryloyldimethyltaurate/VPCopolymer, PEG-60 Hydrogenated Castor Oil, Chlorphenesin, Allantoin, Ethylhexylglycerin, Lavandula Angustifolia(Lavender) Oil, Butylene
Glycol, Hamamelis Virginiana (Witch Hazel) Flower Water, Disodium EDTA, Linalool, Origanum Vulgare Flower Extract, Hibiscus Sabdariffa Flower Extract, Chrysanthemum Indicum Flower Extract, Oenothera Biennis (Evening Primrose) Flower Extract, Camellia Japonica Flower Extract , Hydrolyzed Collagen - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
1) Ask a dermatologist if there are any irritation or side effects
such as red spots, swelling, and itching after using the cosmetics or being exposed to direct sunlight.2) Do not use on damaged or broken skin.
3) Precautions for storage. A) Keep away from
children. B) Keep away from direct sunlight.4) α-hydroxyacid (AHA) containing product
A) Use with sunblock because the product couldincrease skin’s sensitivity to the sunlight.
B) Test on some skin areas to check whether the product causes skin irritation.
5) Do not use it for children under 3 years old.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PAHABA SOLUTION
niacinamide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81715-0004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 5 g in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81715-0004-1 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/04/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/04/2021 Labeler - JH Science Co., Ltd. (695129996) Registrant - JH Science Co., Ltd. (695129996) Establishment Name Address ID/FEI Business Operations JH Science Co., Ltd. 695129996 label(81715-0004) , manufacture(81715-0004)
