Label: RBX FOR MEN ANTIBACTERIAL HAND WASH ALOE VERA AND TEA TREE SCENTED- benzalkonium chloride liquid
- NDC Code(s): 56136-501-01
- Packager: Ganzhou Olivee Cosmetic Co., Ltd.
- 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 November 15, 2020
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Inactive ingredients
Water (Aqua), Cocamidopropyl Betaine, Cocamidopropylamine Oxide, Hydroxethylcellulose, Fragrance (Parfum), Phenoxyethanol, Bezyl Alcohol, PEG-150 Distearate, Sodium Chloride, Glycerin, Citric Acid, Aloe Barbadensis Leaf Etract, Melaleuca alternifolia (Tea Tree) Extract, Tocopheryl Acetate. May contain: FD&C Red No. 4 (C.I. 14700), FD&C Yellow No. 5 (C.I. 19140), D&C Red No. 33 (Cl 17200), FD&C Blue No. 1 (Cl 42090).
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INGREDIENTS AND APPEARANCE
RBX FOR MEN ANTIBACTERIAL HAND WASH ALOE VERA AND TEA TREE SCENTED
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:56136-501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) BENZYL ALCOHOL (UNII: LKG8494WBH) GLYCERIN (UNII: PDC6A3C0OX) ACETYLTRIETHYL CITRATE (UNII: 5WBR36T90E) PHENOXYETHANOL (UNII: HIE492ZZ3T) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) TEA TREE OIL (UNII: VIF565UC2G) ALOE VERA LEAF (UNII: ZY81Z83H0X) FD&C RED NO. 3 (UNII: PN2ZH5LOQY) FD&C RED NO. 4 (UNII: X3W0AM1JLX) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:56136-501-01 350 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 11/15/2020 Labeler - Ganzhou Olivee Cosmetic Co., Ltd. (543008195) Establishment Name Address ID/FEI Business Operations Ganzhou Olivee Cosmetic Co., Ltd. 543008195 manufacture(56136-501)