SALICYLIC 20 SKIN PEEL solution SALICYLIC 30 SKIN PEEL- salicylic 20 skin peel solution

SALICYLIC 30 Skin Peel by

Drug Labeling and Warnings

SALICYLIC 30 Skin Peel 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

Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and

WARNINGS

DIRECTIONS: Apply the peel to the treatment area. Let stand on skin for 2-10 minutes depending on skin tolerance. Remove peel with copious amount of water. Follow with moisturizer. Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and

INACTIVE INGREDIENT

Inactive ingredients: Propylene Glycol, SD Alcohol, Hexylene Glycol.

ACTIVE INGREDIENT

Active ingredient: Salicylic Acid.

KEEP OUT OF REACH OF CHILDREN

keep out of reach of children

INDICATIONS & USAGE

Apply the peel to the treatment area. Let stand on skin for 2-10 minutes depending on skin tolerance. Remove peel with copious amount of water. Follow with moisturizer. Note: A stinging sensation may occur. Flakiness may occur for 3-5 days after performing peel. When using this product avoid unnecessary sun exposure and
use sunscreen.
For external use only.

PURPOSE

salicylic acid skin peel
20%
Removes Blackheads Cleans Pores
Clears Acne & Scars

Distributed By:
Skin Beauty Solutions Elk Grove CA 95759

PRINCIPAL DISPLAY PANEL

Content of labeing

INGREDIENTS AND APPEARANCE

SALICYLIC 20 SKIN PEEL 
salicylic 20 skin peel solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84785-0013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.3 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
CITRAL PROPYLENE GLYCOL ACETAL (UNII: 9W7YHX7EX6)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84785-0013-1	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024
2	NDC: 84785-0013-2	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024
3	NDC: 84785-0013-3	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024
4	NDC: 84785-0013-4	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024
5	NDC: 84785-0013-5	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024
6	NDC: 84785-0013-6	480 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

SALICYLIC 30 SKIN PEEL 
salicylic 20 skin peel solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84785-0014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.3 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
CITRAL PROPYLENE GLYCOL ACETAL (UNII: 9W7YHX7EX6)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84785-0014-1	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024
2	NDC: 84785-0014-2	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024
3	NDC: 84785-0014-3	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024
4	NDC: 84785-0014-4	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024
5	NDC: 84785-0014-5	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2024
6	NDC: 84785-0014-6	480 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(84785-0013, 84785-0014)