AHA GLYCOLIC ACID FOAM CLEANSER- SULFATE-FREE- 7.5 OZ solution

AHA Glycolic Acid Foam Cleanser (Sulfate-Free)- 7.5 oz by

Drug Labeling and Warnings

AHA Glycolic Acid Foam Cleanser (Sulfate-Free)- 7.5 oz by is a Otc medication manufactured, distributed, or labeled by Gazebo Wellness SKIN LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Skin Beauty Solutions Alpha Hydroxy Foam Cleanser removes dirt, excess oil, and impurities without irritating skin.

WARNINGS

Directions: Apply cleanser onto wet faceand neck, massage and rinse with cool water. Use 3-5 times a week. Not recommended for sensitive skin.

INACTIVE INGREDIENT

Inactive Ingredients: Aqua (Water), Decyl Glucoside, Cocamidopropyl Betaine, Kosher Vegetable Glycerin, Phenoxyethanol, Xanthan Gum (Polysaccharide Gum), Tetrasodium EDTA, d-Calcium Pantothenate (Pro-Vitamin B5).

INDICATIONS & USAGE

Directions: Apply cleanser onto wet faceand neck, massage and rinse with cool water. Use 3-5 times a week. Not recommended for sensitive skin.

KEEP OUT OF REACH OF CHILDREN

keep out of reach of children

PURPOSE

SKINBEAUTY
SOLUTIONS-
AHA Foam Cleanser
with Glyolic Acid
Removes Dirt Excess Oil
& Impurities
Distributed By:
Skin Beauty Solutions Elk Grove CA 95759

ACTIVE INGREDIENT

Active Ingredient: Glycolic Acid.

PRINCIPAL DISPLAY PANEL

Content of Labeling

INGREDIENTS AND APPEARANCE

AHA GLYCOLIC ACID FOAM CLEANSER (SULFATE-FREE)- 7.5 OZ 
aha glycolic acid foam cleanser (sulfate-free)- 7.5 oz solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84785-0027
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCOLIC ACID (UNII: 0WT12SX38S) (GLYCOLIC ACID - UNII:0WT12SX38S)	GLYCOLIC ACID	22.5 mg  in 225 mL

Inactive Ingredients
Ingredient Name	Strength
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
GLYCERIN (UNII: PDC6A3C0OX)
AQUA (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TETRASODIUM EDTA (UNII: MP1J8420LU)
CALCIUM PANTOTHENATE (UNII: 568ET80C3D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84785-0027-1	225 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	10/01/2024

Labeler - Gazebo Wellness SKIN LLC (119609953)

Registrant - Gazebo Wellness SKIN LLC (119609953)

Establishment
Name	Address	ID/FEI	Business Operations
Gazebo Wellness SKIN LLC		119609953	manufacture(84785-0027)