Label: ANTIBACTERIAL SKIN CLEANSER- chloroxylenol soap
- NDC Code(s): 72024-708-04
- Packager: Fastenal
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 2, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Uses
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Warnings
- For external use only.
- Avoid contact with eyes.
- Children under the age of 6 should be supervised by an adult when using this product.
- Discontinue use is irritation or redness develops.
- 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
- Purpose
- KEEP OUT OF REACH OF CHILDREN
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTIBACTERIAL SKIN CLEANSER
chloroxylenol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72024-708 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 4 mg in 1 mL Inactive Ingredients Ingredient Name Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) ALCOHOL (UNII: 3K9958V90M) D&C GREEN NO. 5 (UNII: 8J6RDU8L9X) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) MAGNESIUM NITRATE (UNII: 77CBG3UN78) DIMETHYL BENZYL CARBINYL BUTYRATE (UNII: 3Q0C60547R) ETHYL BUTYRATE (UNII: UFD2LZ005D) SODIUM FERROCYANIDE (UNII: 5HT6X21AID) ETHYL ACETOACETATE (UNII: IZP61H3TB1) LAURIC ISOPROPANOLAMIDE (UNII: 82DUX3RRVU) SODIUM CARBONATE (UNII: 45P3261C7T) GLYCOL DISTEARATE (UNII: 13W7MDN21W) .GAMMA.-DECALACTONE (UNII: 7HLS05KP9O) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) ETHYL METHYLPHENYLGLYCIDATE (UNII: UD51D5KR4A) CHLOROACETIC ACID (UNII: 5GD84Y125G) IONONE (UNII: QP734LIN1K) BENZYL BENZOATE (UNII: N863NB338G) MYRCENE (UNII: 3M39CZS25B) SODIUM HYDROXIDE (UNII: 55X04QC32I) METHYL ANTHRANILATE (UNII: 981I0C1E5W) DIMETHYL BENZYL CARBINYL ACETATE (UNII: 6Y9488RL8H) CALCIUM SILICATE (UNII: S4255P4G5M) SODIUM LAURYL SULFATE (UNII: 368GB5141J) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYL ALCOHOL (UNII: Y4S76JWI15) ETHYLENE OXIDE (UNII: JJH7GNN18P) LINALOOL, (+/-)- (UNII: D81QY6I88E) DIOXANE (UNII: J8A3S10O7S) TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) SODIUM ALUMINIUM SILICATE (UNII: 058TS43PSM) WATER (UNII: 059QF0KO0R) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PHENOXYETHANOL (UNII: HIE492ZZ3T) COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72024-708-04 3780 mL in 1 JUG; 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 Drug 505G(a)(3) 11/12/2012 Labeler - Fastenal (042653634) Registrant - Betco corporation, Ltd. (005050158) Establishment Name Address ID/FEI Business Operations Betco Corporation, Ltd. 005050158 label(72024-708) , manufacture(72024-708)
