BARUBT INTENSIVE PEELING SOLUTION- intensive peeling solution lotion

BARUBT Intensive Peeling Solution by

Drug Labeling and Warnings

BARUBT Intensive Peeling Solution 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

Glycolic acid 0.5%
sallcylic acid 0.5%
lactic acid 0.5%
panthenol 0.05%

DO NOT USE

on damaged or broken skin

KEEP OUT OF REACH OF CHILDREN

Keep away from children. Do not swallow.

PURPOSE

Softens and cleanses the aged keratin on the skin surface

QUESTIONS

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

STOP USE

Discontinue use and clean with clear water immediately if redness or skin irritation occurs.

WHEN USING

keep out of eyes. Rinse with water to remove.

INACTIVE INGREDIENT

Aqua(water)
1.2-Hexanediol
1,3-Propanedi-ol
tartaric acid
Carrot (DAUCUS CAROTASATIVA) extract
citric acid
Cocamidopro-pyl Dimethylamine
xanthan gum
Sodiumhyaluronate cross-linked polymer
Caprylyl Glycol
Potassium Sorbate
Ethyl-hexylglycerin
sodium benzoate
glycerin
sodium hydroxide
False staranise/leaf extract
Aloe vera(ALOEBARBADENSIS) leaf water
Spring water
1,2-pentanediol
Polysorbate-20
Trisodiumethylenediamine disuccinate

DOSAGE & ADMINISTRATION

Wet the skin and apply an appropriate amount to the face, avoiding the eye area.Rub gently for 10-30 seconds until the old cuticle is rubbed out, then rinse off with water, use once or twice a week.

STORAGE AND HANDLING

Keep away from light and in adry place.

WARNINGS

For external use only.

INDICATIONS & USAGE

Softens and cleanses the aged keratin on the skin surface, moisturizes and improves the roughness of the skin surface, cleanses the pores and gives the skin a comfortable and translucent feeling

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BARUBT INTENSIVE PEELING SOLUTION 
intensive peeling solution lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84712-011
Route of Administration	TOPICAL, CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z)	PANTHENOL	0.0175 g  in 35 mL
LACTIC ACID (UNII: 33X04XA5AT) (LACTIC ACID - UNII:33X04XA5AT)	LACTIC ACID	0.175 g  in 35 mL
GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S)	GLYCOLIC ACID	0.175 g  in 35 mL

Inactive Ingredients
Ingredient Name	Strength
XANTHAN GUM (UNII: TTV12P4NEE)	0.035 g  in 35 mL
TARTARIC ACID (UNII: W4888I119H)	0.07 g  in 35 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84712-011-01	35 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/12/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/12/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Youbaijia Cosmetic Industry Co., Ltd		702314361	manufacture(84712-011) , label(84712-011)