Pahaba Control

Manufacturer
JH Science Co., Ltd.
Effective date
2021-04-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:47:51

Label at a glance#

ProductPahaba Control
Active ingredientNIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

niacinamide

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

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 SECTION

external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81715-000181715-0001-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
NIACINAMIDE25X51I8RD4ACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
27b3fcf9-2e38-0aeb-e063-6394a90abff1bf1f1d7a-5629-4f98-e053-2a95a90a689a2024-11-24WarningsExact identifier
spl set id: bf1f1d7a-5629-4f98-e053-2a95a90a689a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.