PAHABA CONTROL- niacinamide liquid

Pahaba Control by

Drug Labeling and Warnings

Pahaba Control by is a Otc medication manufactured, distributed, or labeled by JH Science Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

niacinamide

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

strengthen the skin and protect the skin from harmful external environments making it healthy

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Every evening after a facial cleansing, apply Pahaba Control on your face and pat for more than 3 minutes for thorough absorption.

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

external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PAHABA CONTROL 
niacinamide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81715-0001
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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81715-0001-1	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(81715-0001) , manufacture(81715-0001)