MELAO GLYCOLIC ACID PEEL 70%- butylene glycol liquid

MELAO GLYCOLIC ACID PEEL 70% by

Drug Labeling and Warnings

MELAO GLYCOLIC ACID PEEL 70% by is a Otc medication manufactured, distributed, or labeled by Guangzhou Yilong Cosmetics Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Dipotassium Glycyrrhizate 2%

Glycerin4%

Inactive ingredients

Water 60%

Butylene Glycol15%

Propylene Glycol5%

Sodium Hyaluronate4%

Allantoin3%

Panthenol2%

Xanthan Gum2%

Dipotassium Glycyrrhizate2%

Glyceryl Polymetha crylate2%

Saccharum Officinarum (Sugarcane) Extract0.5%

Fragrance0.5%

Purpose

Moisture

Uses

Step 1: Clean and thoroughly dry your skin.
Step 2: Rotate the bottle cap to open the product.
Step 3: Gently apply to the surface of the skin.

Warnings

For external use only.

Stop use and ask a doctor if

rash occurs.

Do not use

on damaged or broken skin.

When using this product

keep out of eyes. Rinse withwater to remove.

Keep out of reach of children.

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Squeeze out an appropriate amount of sunscreen and spread evenly on skin.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MELAO GLYCOLIC ACID PEEL 70% 
butylene glycol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83566-570
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	4 g  in 100 g
DIPOTASSIUM GLUCARATE (UNII: U9GJZ222NU) (DIPOTASSIUM GLUCARATE - UNII:U9GJZ222NU)	DIPOTASSIUM GLUCARATE	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER O-18 (UNII: 7QV8F8BYNJ)	60 g  in 100 g
ALLANTOIN BIOTIN (UNII: 8445SU9RKR)	3 g  in 100 g
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER (UNII: 788QAG3W8A)	4 g  in 100 g
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)	15 g  in 100 g
DIPROPYLENE GLYCOL CAPRYLATE (UNII: CJ981S4H3T)	5 g  in 100 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83566-570-01	30 g in 1 BOTTLE; Type 0: Not a Combination Product	08/08/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	08/08/2024

Labeler - Guangzhou Yilong Cosmetics Co., Ltd (712647107)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Yilong Cosmetics Co., Ltd		712647107	manufacture(83566-570)