Label: SANIFOAM HAND SANITIZER- alcohol lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 50536-039-01 - Packager: AMERICAN CHEMICAL AND SANITARY SUPPLY 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 15, 2022
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- ACTIVE INGREDIENT
- PURPOSE
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WARNINGS
FIRST AID:
EYES: AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER. CALL PHYSICIAN IF IRRITATION OR REDNESS DEVELOPS AND LASTS.
INGESTION: IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL OR CONTACT A POISON CNTROL CENTER IMMEDIATELY.
CONTAINER DISPOSAL: RINSE THREE TIMES WITH WATER. THEN OFFER FOR RECYCLING OR RECONDITIONING OR PUNCTURE AND DISPOSE OF IN A SANITARY LANDFILL OR BY INCARCERATION OR, IF ALLOWED BY STATE AND LOCAL AAUTHORITIES, BY BURNING. IF BURNED, STAY AWAY FROM SMOKE.
- INDICATIONS & USAGE
- KEEP OUT OF REACH OF CHILDREN
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SANIFOAM HAND SANITIZER
alcohol lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50536-039 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50536-039-01 3785 mL in 1 JUG; Type 0: Not a Combination Product 03/12/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/12/2014 Labeler - AMERICAN CHEMICAL AND SANITARY SUPPLY INC (177148699)