Label: ANTIBACTERIAL- chloroxylenol liquid
- NDC Code(s): 55319-956-42, 55319-956-44
- Packager: Family Dollar
- Category: HUMAN OTC DRUG LABEL
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 September 13, 2022
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
-
Inactive ingredients
water, sodium C14-16 olefin sulfonate, lauramine oxide and/or lauramidopropylamine oxide and myristamidopropylamine oxide, sodium laureth sulfate, sodium lauryl sulfate, sodium chloride, sodium xylenesulfonate, alcohol denat., fragrance, phenoxyethanol, citric acid, methylisothiazolinone, tetrasodium EDTA, yellow 5, blue 1
-
claims
- Do not add bleach.
- Not for use in dishwashers.
- Contains surfactants
- Phosphate free
- This product is not manufactured or distributed by Procter & Gamble, distributor of Dawn Ultra Antibacterial Hand Soap Apple Blossom Scent.
NOT 100% SATISFIED? Return packaged and unused product within 30 days to any Family Dollar store for a refund (with receipt) or exchange.
- Adverse reaction
- principal display panel
-
INGREDIENTS AND APPEARANCE
ANTIBACTERIAL
chloroxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55319-956 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 3.09 mg in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T) sodium laureth sulfate (UNII: BPV390UAP0) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) ALCOHOL (UNII: 3K9958V90M) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) DITETRACYCLINE TETRASODIUM EDETATE (UNII: WX0A0IT7K5) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55319-956-44 531 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 04/29/2016 2 NDC:55319-956-42 828 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 04/29/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/29/2016 Labeler - Family Dollar (024472631) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(55319-956) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(55319-956)
