Pahaba Solution: Package Insert and Label Information

PAHABA SOLUTION- niacinamide and adenosine liquid
JH Science Co., Ltd.

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.

niacinamide, adenosine

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

to improve elasticity, skin whitening effects

keep out of reach of the children

after washing your face every evening, apply it on your face and pat for more thqan 3 minutes to absorb thoroughly

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.

external use only

(click image for full-size original)

niacinamide liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:81715-0004
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Inactive Ingredients
Ingredient Name Strength
# Item Code Package Description Multilevel Packaging
1 NDC:81715-0004-1 50 mL in 1 BOTTLE None
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)
Name Address ID/FEI Operations
JH Science Co., Ltd. 695129996 label (81715-0004), manufacture (81715-0004)

Revised: 04/2021 JH Science Co., Ltd. provides trustworthy package insert and label information about marketed drugs as submitted by manufacturers to the US Food and Drug Administration. Package information is not reviewed or updated separately by Every individual package label entry contains a unique identifier which can be used to secure further details directly from the US National Institutes of Health and/or the FDA.

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