Home NDC 61010-8600-01 NDC 61010-8600-01 - Saniwash Antimicrobial Foaming Hand This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 61010-8600
Requested NDC 61010-8600-01
Package NDCs from labels 61010-8600-1, 61010-8600-01
Manufacturer Safetec of America, Inc. | Safetec of America, Inc
Effective date 2024-02-04
Current FDA listing Not matched in FDA.report NDC product tables FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61010-8600-1 Saniwash Antimicrobial Foaming Hand 550 mL in 1 BOTTLE, PUMP LIQUID 550 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61010-8600 SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20240214_bab4ca5f-01c6-4146-b18f-c22cbe0fe13b.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Chloroxylenol ACTIVE INGREDIENT 0F32U78V2Q SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC. ] 1 Chloroxylenol ACTIVE MOIETY 0F32U78V2Q SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC. ] 1 .ALPHA.-TOCOPHEROL ACETATE INACTIVE INGREDIENT 9E8X80D2L0 SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC. ] 1 Aloe Vera Leaf INACTIVE INGREDIENT ZY81Z83H0X SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC. ] 1 Cocamidopropyl Betaine INACTIVE INGREDIENT 5OCF3O11KX SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC. ] 1 COCO DIETHANOLAMIDE INACTIVE INGREDIENT 92005F972D SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC. ] 1 DMDM HYDANTOIN INACTIVE INGREDIENT BYR0546TOW SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC. ] 1 EDETATE SODIUM INACTIVE INGREDIENT MP1J8420LU SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC. ] 1 Propylene Glycol INACTIVE INGREDIENT 6DC9Q167V3 SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC. ] 1 SODIUM LAURETH-3 SULFATE INACTIVE INGREDIENT BPV390UAP0 SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC. ] 1 Water INACTIVE INGREDIENT 059QF0KO0R SANIWASH ANTIMICROBIAL FOAMING HAND (CHLOROXYLENOL) LIQUID [SAFETEC OF AMERICA, INC. ] 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 9 of 27 · 537 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.