SALICYLIC FOAM CLEANSER 20% 7.5 OZ solution

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]

DOSAGE & ADMINISTRATION

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

WARNINGS

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

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 face and neck, massage and rinse with cool water, Use 3-5 times a week.

KEEP OUT OF REACH OF CHILDREN

keep out of reach of children

PURPOSE

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

Active Ingredient:

Salicylic Acid.

PRINCIPAL DISPLAY PANEL

Content of Labeling

INGREDIENTS AND APPEARANCE

SALICYLIC FOAM CLEANSER 20% 7.5 OZ 
salicylic foam cleanser 20% 7.5 oz solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84785-0028
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	22.5 mg  in 225 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84785-0028-1	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(84785-0028)