Label: GLYCOLIC ACID- pari 30% glycolic acid peel liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 81376-701-01 - Packager: SSG Ventures Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated April 7, 2021
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PRINCIPAL DISPLAY PANEL
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.
DIRECTIONS
Cleanse area to be exfoliatedUse 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
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 -
INGREDIENTS AND APPEARANCE
GLYCOLIC ACID
pari 30% glycolic acid peel liquidProduct 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)