Label: GLO SKIN BEAUTY CLEAR SKIN CLEANSER liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 60541-1700-2 - Packager: Hayden Caleel LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 28, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
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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
- Directions
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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
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INGREDIENTS AND APPEARANCE
GLO SKIN BEAUTY CLEAR SKIN CLEANSER
glo skin beauty clear skin cleanser liquidProduct 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)
