BARUBT OCEAN PORE CLAY STICK- ocean pore clay stick paste

BARUBT Ocean Pore Clay Stick by

Drug Labeling and Warnings

BARUBT Ocean Pore Clay Stick by is a Otc medication manufactured, distributed, or labeled by Guangdong Youbaijia Cosmetic Industry Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

NIACINAMIDE 1%
CENTELLA ASIATICA LEAF EXTRACT 0.035%
GLYCYRRHIZA URALENSIS (LICORICE) EXTRACT 0.035%
GLYCOLIC ACID 0.05%

INACTIVE INGREDIENT

WATER
GLYCERIN
PROPYLENE GLYCOL
KAOLIN
DIATQMACEOUS EARTH
PALMITIC ACID
STEARIC ACID
SODIUM HYBROXIDE
CI 77288
METHYLPARABEN
DMDM HYDANTOIN
DISODIUM EDTA
PARFUM
BUTYLENE GLYCOL
SEA GRAPE
DEEP OCEAN WATER
CI42090
MENTHA HAPLOCALYX EXTRACT
HYDROXVACETOPHENONE

DO NOT USE

Do not use on damaged skin.

KEEP OUT OF REACH OF CHILDREN

Keep away from children. Do not swallow.

PURPOSE

moisturizing and cleaning

QUESTIONS

Contact name: Jessie Peng
Company phone number: +1 818 579 7288
Company e-mail: jessie@registeragentllc.com

STOP USE

lf you feel uncomfortable or have abnormal skin reactions during use, please stop using or consult a dermatologist.

WHEN USING

keep out of eyes. Rinse with water to remove.

WARNINGS

For external use only.

STORAGE AND HANDLING

Keep away from light and in a dry place.

INDICATIONS & USAGE

Contains a variety of extracts and moisturizing essences, the texture is refreshing and moisturizing;delicately cleans the facial skin,helping to absorb excess oil, dust and other dirt on the skin surface and pores; and purifies the pores while the skin is fresh and not tight, leaving the skin fresh Pure and moisturizing, soft and smooth, with a translucent and clean radiance

DOSAGE & ADMINISTRATION

First, wash the face with facial cleanser, apply appropriate amount of this product evenly on the face, avoid the eyes and lips, leave for 15-20 minutes, after the mud film dries, rinse with water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BARUBT OCEAN PORE CLAY STICK 
ocean pore clay stick paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84712-019
Route of Administration	CUTANEOUS, TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CENTELLA ASIATICA LEAF (UNII: 6810070TYD) (CENTELLA ASIATICA LEAF - UNII:6810070TYD)	CENTELLA ASIATICA LEAF	0.014 g  in 40 g
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	0.4 g  in 40 g
GLYCYRRHIZA URALENSIS (UNII: 42B5YD8F0K) (GLYCYRRHIZA URALENSIS - UNII:42B5YD8F0K)	GLYCYRRHIZA URALENSIS	0.014 g  in 40 g
GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S)	GLYCOLIC ACID	0.02 g  in 40 g

Inactive Ingredients
Ingredient Name	Strength
STEARIC ACID (UNII: 4ELV7Z65AP)	1.6 g  in 40 g
PALMITIC ACID (UNII: 2V16EO95H1)	2.4 g  in 40 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84712-019-01	40 g in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/17/2024

Labeler - Guangdong Youbaijia Cosmetic Industry Co., Ltd (702314361)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Youbaijia Cosmetic Industry Co., Ltd		702314361	label(84712-019) , manufacture(84712-019)