GLYCOLIC ACID- pari 30% glycolic acid peel liquid

Glycolic Acid by

Drug Labeling and Warnings

Glycolic Acid by is a Otc medication manufactured, distributed, or labeled by SSG Ventures Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

INGREDIENTS

Glycolic Acid

FOR SKIN PRONE TO BREAKOUTS
FOR AGING SKIN

Keep out of reach of children.

CAUTION
For external use only. Avoid contact with eyes and\ mucous membranes. In case of contact with eyes, flush with water. Some users may experience mild skin irritation. If irritation or redness lingers after rinsing, discontinue use and seek medical attention. Use caution when applying a solution stronger than 10% below the neckline. Keep out of reach of children.

FOR SKIN PRONE TO BREAKOUTS
FOR AGING SKIN

DIRECTIONS
Cleanse area to be exfoliated

Use sterile gauze to apply a thin layer of acid peel to the skin

Wait for 60 to 90 seconds (20 seconds for first use; 20 to 60 seconds on sensitive skin)

Rinse with cool water

Repeat weekly until desired results

Apply sunscreen to any exfoliated areas for extra protection

Hydroxyethyl Cellulose, Preserved Water

Cleanse area to be exfoliated

Use sterile gauze to apply a thin layer of acid peel to the skin

Wait for 60 to 90 seconds (20 seconds for first use; 20 to 60 seconds on sensitive skin)

Rinse with cool water

Repeat weekly until desired results

Apply sunscreen to any exfoliated areas for extra protection

FOR SKIN PRONE TO BREAKOUTS
FOR AGING SKIN

INGREDIENTS AND APPEARANCE

GLYCOLIC ACID 
pari 30% glycolic acid peel liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81376-701
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S)	GLYCOLIC ACID	9 g  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)

Product Characteristics
Color	yellow (clear)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81376-701-01	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	04/12/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/12/2021

Labeler - SSG Ventures Inc (047626115)

Establishment
Name	Address	ID/FEI	Business Operations
SSG Ventures Inc		047626115	manufacture(81376-701)