Label: ANTIBACTERIAL MOISTURIZING HAND LOTION SUN BLOSSOM- benzalkonium chloride lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 59779-339-03 - Packager: CVS PHARMACY
- 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 May 18, 2011
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- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- DIRECTIONS
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INACTIVE INGREDIENTS
WATER, CYCLOPENTASILOXANE, GLYCINE SOJA (SOYBEAN) OIL, GLYCERIN, CETEARYL ALCOHOL, CETEARETH-20, GLYCERYL STEARATE, DIMETHICONE, CETYL ALCOHOL, STEARYL ALCOHOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, ETHYLHEXYL PALMITATE, DICAPRYLYL CARBONATE, THEOBROMA CACAO (COCOA) SEED BUTTER, FRAGRANCE, HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, ETHYLHEXYL METHOXYCINNAMATE, BUTYL METHOXYDIBENZOYLMETHANE, ETHYLHEXYL SALICYLATE, PPG-26-BUTETH-26, PEG-40 HYDROGENATED CASTOR OIL, DMDM HYDANTOIN, MANNITOL, CELLULOSE, MICA, TITANIUM OXIDE (CI 77891), IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), RED 40 (CI 16035), YELLOW 5 (CI 19140).
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL MOISTURIZING HAND LOTION SUN BLOSSOM
benzalkonium chloride lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-339 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) SOYBEAN OIL (UNII: 241ATL177A) GLYCERIN (UNII: PDC6A3C0OX) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) DIMETHICONE (UNII: 92RU3N3Y1O) CETYL ALCOHOL (UNII: 936JST6JCN) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ETHYLHEXYL PALMITATE (UNII: 2865993309) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) COCOA BUTTER (UNII: 512OYT1CRR) SUNFLOWER SEED (UNII: R9N3379M4Z) MICA (UNII: V8A1AW0880) OCTINOXATE (UNII: 4Y5P7MUD51) AVOBENZONE (UNII: G63QQF2NOX) OCTISALATE (UNII: 4X49Y0596W) POLYOXYL 40 CASTOR OIL (UNII: 4ERD2076EF) DMDM HYDANTOIN (UNII: BYR0546TOW) MANNITOL (UNII: 3OWL53L36A) POWDERED CELLULOSE (UNII: SMD1X3XO9M) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) HYPROMELLOSES (UNII: 3NXW29V3WO) CHROMIC OXIDE (UNII: X5Z09SU859) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-339-03 72 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/18/2011 Labeler - CVS PHARMACY (062312574) Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209) Establishment Name Address ID/FEI Business Operations APOLLO HEALTH AND BEAUTY CARE 201901209 manufacture