Label: SIGNATURE HOME AB ORANGE- chloroxylenol soap
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Contains inactivated NDC Code(s)
NDC Code(s): 63691-027-10 - Packager: Sun Products Corporation
- 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 June 29, 2016
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Dishwashing Liquid & Antibacterial Hand Soap
- Active Ingredient
- Purpose
- Use
- Warnings
- Keep out of reach of children
- Directions
- Inactive ingredients
- Questions?
- Signature Home Orange AB-page-001.jpg
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INGREDIENTS AND APPEARANCE
SIGNATURE HOME AB ORANGE
chloroxylenol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63691-027 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.3 g in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM XYLENESULFONATE (UNII: G4LZF950UR) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) ALCOHOL (UNII: 3K9958V90M) EDETATE SODIUM (UNII: MP1J8420LU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) D&C RED NO. 33 (UNII: 9DBA0SBB0L) WATER (UNII: 059QF0KO0R) BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y) SODIUM CHLORIDE (UNII: 451W47IQ8X) Product Characteristics Color Score Shape Size Flavor ORANGE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63691-027-10 709 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/30/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 04/30/2016 Labeler - Sun Products Corporation (070931480) Registrant - Safeway (009137209)