Salicylic Foam Cleanser 20% 7.5 oz by Gazebo Wellness SKIN LLC

Salicylic Foam Cleanser 20% 7.5 oz by

Drug Labeling and Warnings

Salicylic Foam Cleanser 20% 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]

SALICYLIC FOAM CLEANSER 20% 7.5 OZ- salicylic foam cleanser 20% 7.5 oz solution 
Gazebo Wellness SKIN LLC

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Skin Beauty Solutions Salicylic Foam, Removes dirt, dead skin, and oil from pores that can cause active acne.

Directions: Apply cleanser onto wet face and neck, massage and rinse with cool water, Use 3-5 times a week.

Inactive Ingredients:

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

Directions: Apply cleanser onto wet face and neck, massage and rinse with cool water, Use 3-5 times a week.

keep out of reach of children

SKINBEAUTY
SOLUTIONS-
Salicylic Foam Cleanser
20%
Removes dirt, dead skin, and oil from pores.

Distributed By: Skin Beauty Solutions Woodbury MN 55129
7.5oz/225 ml
MADE INUSA 12M

Active Ingredient:

Salicylic Acid.

Content of Labeling

Content of labeling 225 ml

SALICYLIC FOAM CLEANSER 20% 7.5 OZ 
salicylic foam cleanser 20% 7.5 oz solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 84785-0028
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID22.5 mg  in 225 mL
Inactive Ingredients
Ingredient NameStrength
XANTHAN GUM (UNII: TTV12P4NEE)  
CALCIUM PANTOTHENATE (UNII: 568ET80C3D)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
AQUA (UNII: 059QF0KO0R)  
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
TETRASODIUM EDTA (UNII: MP1J8420LU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 84785-0028-1225 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01610/01/202409/30/2025
Labeler - Gazebo Wellness SKIN LLC (119609953)
Registrant - Gazebo Wellness SKIN LLC (119609953)
Establishment
NameAddressID/FEIBusiness Operations
Gazebo Wellness SKIN LLC119609953manufacture(84785-0028)

Revised: 9/2025