Label: AMERIWASH- parachlorometaxylenol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 52410-8038-3, 52410-8038-4, 52410-8038-5 - Packager: SHIELD LINE LLC
- 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 January 13, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Inactive Ingredients
- AMERIWASH DRUG FACT PANEL
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INGREDIENTS AND APPEARANCE
AMERIWASH
parachlorometaxylenol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52410-8038 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 0.003 mg in 1 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) COCO DIETHANOLAMIDE (UNII: 92005F972D) DMDM HYDANTOIN (UNII: BYR0546TOW) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) WATER (UNII: 059QF0KO0R) D&C RED NO. 33 (UNII: 9DBA0SBB0L) SULISOBENZONE (UNII: 1W6L629B4K) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52410-8038-3 800 mL in 1 POUCH; Type 0: Not a Combination Product 08/01/2017 2 NDC:52410-8038-4 1000 mL in 1 POUCH; Type 0: Not a Combination Product 08/01/2017 3 NDC:52410-8038-5 3780 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 08/01/2017 Labeler - SHIELD LINE LLC (078518916)