GLO SKIN BEAUTY CLEAR SKIN CLEANSER liquid

glo SKIN BEAUTY Clear Skin Cleanser by

Drug Labeling and Warnings

glo SKIN BEAUTY Clear Skin Cleanser by is a Otc medication manufactured, distributed, or labeled by Hayden Caleel LLC, Swiss-American CDMO, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Salicylic Acid 2%

Purpose

Acne Treatment

Uses

• Treats Acne
• Helps prevent the development of new acne blemishes

Warnings

Using other topical acne medications at the same tiem or immediatly following use of this prouct may increase dryness or irritation of the skin. If this occurs, only one medication shoul be used unless directed by a doctor.

For external use only
When using this product
avoid contact with the eyes
if contact occurs, rinse thoroughly with water
do not use on damaged or broken skin

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help
or contact a Poison Control Center right away.

Directions

• Use once or twice daily to cleanse skin thoroughly
• Dispense a small amount onto dampened face
• Massage gently for up to 60 seconds
• Rinse thoroughly with water, towel dry
• If bothersome dryness or peeling occurs, reduce use to once a day or every other ay

Inactive Ingredients

Aqua/Water/Eau, Sodium Cocoyl Apple Amino Acids, Cocamidopropyl Betaine, Sodium Cocoyl Isethionate, Synthetic Wax, Magnesium Silicate, Polyacrylate-13, Methyl Perfluoroisobutyl Ether, Methyl Perfluorobutyl Ether, Polyisobutene, Polysorbate 20, Polyhydroxystearic Acid, Isononyl Isononanoate, Ethylhexyl Isononanoate, Sodium Cocamidopropyl PG-Dimonium Chloride Phosphate, Xanthan Gum, Disodium EDTA, Phenoxyethanol, Sodium Bisulfite, Sodium Hydroxide, Parfum/Fragrance, Butylene Glycol, Iodopropynyl Butylcarbamate, Limonene

Principal Display Panel

INGREDIENTS AND APPEARANCE

GLO SKIN BEAUTY CLEAR SKIN CLEANSER 
glo skin beauty clear skin cleanser liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60541-1700
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM COCO-SULFATE (UNII: 3599J29ANH)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)
MAGNESIUM SILICATE (UNII: 9B9691B2N9)
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
METHYL PERFLUOROISOBUTYL ETHER (UNII: HI89P35AAX)
METHYL PERFLUOROBUTYL ETHER (UNII: H637A50B7U)
POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)
XANTHAN GUM (UNII: TTV12P4NEE)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM BISULFITE (UNII: TZX5469Z6I)
SODIUM HYDRIDE (UNII: 23J3BHR95O)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60541-1700-2	1 in 1 CARTON	12/31/2017
1		200 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	11/30/2017

Labeler - Hayden Caleel LLC (011367468)

Registrant - Hayden Caleel LLC (011367468)

Establishment
Name	Address	ID/FEI	Business Operations
Swiss-American CDMO, LLC		080170933	manufacture(60541-1700)