Label: GLACIER BLUE ANTIBACTERIAL FOAMING SKIN CLEANSER- benzalkonium chloride soap
- NDC Code(s): 62428-759-03, 62428-759-29
- Packager: Lawson Products, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 July 30, 2020
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
-
Warnings
- For external use only. Do not ingest.
- Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
- Stop use and ask a doctor if irritation and redness develop.
- If irritation persists for more than 72 hours, consult a physician.
- KEEP OUT OF REACH OF CHILDREN.
- If swallowed, get medical help or contact a Poison Control Center right away.
- Directions
-
Inactive Ingredients
Water, Phenoxyethanol, Cocamine Oxide, Propylene Glycol, Decyl Glucoside, PEG-4 Rapeseedamide, Cocamidopropyl Hydroxysultaine, Glycerin, Fragrance, Sodium Chloride, Tetrasodium EDTA, Citric Acid, Ethanol, Iodopropynyl Butylcarbamate, Benzyl Acetate, Sodium Glycolate, Sodium Hydroxide, Trisodium Nitrilotriacetate, Diethyl Phthalate, FD&C Blue #1.
- QUESTIONS
- Glacier Ultra Blue Antibacterial Foaming Skin Cleanser
- Glacier Blue Antibacterial Foaming Skin Cleanser
- Glacier Blue Antibacterial Foaming Skin Cleanser
-
INGREDIENTS AND APPEARANCE
GLACIER BLUE ANTIBACTERIAL FOAMING SKIN CLEANSER
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62428-759 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMINE OXIDE (UNII: QWA2IZI6FI) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PEG-4 RAPESEEDAMIDE (UNII: 89575CN928) COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CHLORIDE (UNII: 451W47IQ8X) EDETATE SODIUM (UNII: MP1J8420LU) ALCOHOL (UNII: 3K9958V90M) BENZYL ACETATE (UNII: 0ECG3V79ZJ) SODIUM GLYCOLATE (UNII: B75E535IMI) SODIUM HYDROXIDE (UNII: 55X04QC32I) TRISODIUM NITRILOTRIACETATE (UNII: E3C8R2M0XD) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) 2,4-DIMETHYL-3-CYCLOHEXENE CARBOXALDEHYDE (UNII: 452GFV2AFS) METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y) CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0) MAGNESIUM NITRATE (UNII: 77CBG3UN78) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) GERANIOL (UNII: L837108USY) LIME OIL (UNII: UZH29XGA8G) 2-METHYLUNDECANAL (UNII: S94QNS2VY5) .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF) ALLYL CYCLOHEXANEPROPIONATE (UNII: H4W9H3L241) GERANYL ACETATE (UNII: 3W81YG7P9R) CITRONELLYL ACETATE (UNII: IZ420RT3OY) LINALOOL, (+/-)- (UNII: D81QY6I88E) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) CITRAL (UNII: T7EU0O9VPP) FORMALDEHYDE (UNII: 1HG84L3525) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62428-759-29 1000 mL in 1 BAG; Type 0: Not a Combination Product 11/12/2012 2 NDC:62428-759-03 750 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/12/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 11/12/2012 Labeler - Lawson Products, Inc (005438890) Registrant - Betco Corporation, Ltd (024492831) Establishment Name Address ID/FEI Business Operations Betco Corporation, Ltd 024492831 manufacture(62428-759) , label(62428-759)