Label: ALPET E2 SANITIZING FOAM- chloroxylenol soap
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NDC Code(s):
59900-208-01,
59900-208-02,
59900-208-03,
59900-208-04, view more59900-208-05, 59900-208-06, 59900-208-07, 59900-208-08, 59900-208-09
- Packager: Best Sanitizer, Inc.
- 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 4, 2019
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
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KEEP OUT OF REACH OF CHILDREN
Keep out of reach of children.
In case of eye contact, flush with water for 15 minutes, if irritation persists, get medical attention.
In case of accidental ingestion, seek medical attention or contact a poison control center immediately.
This product must be dispensed from an adequate dispenser located a sufficient distance from processing line to prevent accidental product contamination.
Do not contaminate water, food or feed by storage and disposal. - Directions
- Other information
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALPET E2 SANITIZING FOAM
chloroxylenol soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59900-208 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 15 g in 1000 mL Inactive Ingredients Ingredient Name Strength SODIUM LAURETH SULFATE (UNII: BPV390UAP0) WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) PHENOXYETHANOL (UNII: HIE492ZZ3T) GLYCERIN (UNII: PDC6A3C0OX) TRICLOSAN (UNII: 4NM5039Y5X) EDETATE SODIUM (UNII: MP1J8420LU) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59900-208-01 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2008 2 NDC:59900-208-02 208175 mL in 1 DRUM; Type 0: Not a Combination Product 02/01/2008 3 NDC:59900-208-03 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2008 4 NDC:59900-208-04 1000 mL in 1 BAG; Type 0: Not a Combination Product 02/01/2008 5 NDC:59900-208-05 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2008 6 NDC:59900-208-06 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2008 7 NDC:59900-208-07 2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2008 8 NDC:59900-208-08 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2008 9 NDC:59900-208-09 946250 mL in 1 DRUM; Type 0: Not a Combination Product 02/01/2008 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 02/01/2008 Labeler - Best Sanitizer, Inc. (957473614) Establishment Name Address ID/FEI Business Operations Best Sanitizer, Inc. 627278224 manufacture(59900-208)