Home NDC 59900-217 SoftenSure Antimicrobial Liquid
Product NDC 59900-217
11-digit product format 599000217
Labeler code 59900
Product ID 59900-217_2929d297-4264-0d9a-e063-6294a90a762e
Type HUMAN OTC DRUG
Nonproprietary name Chloroxylenol
Dosage form LIQUID
Route TOPICAL
Labeler Best Sanitizers, Inc
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-12-26
Substance CHLOROXYLENOL
Active strength .75 mg/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base SoftenSure Antimicrobial Liquid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CHLOROXYLENOL .75 mg/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0F32U78V2Q Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59900-217-01 SoftenSure Antimicrobial Liquid 500 mL in 1 BOTTLE LIQUID 500 1 59900-217-02 SoftenSure Antimicrobial Liquid 500 mL in 1 BOTTLE LIQUID 500 1 59900-217-02 SoftenSure Antimicrobial Liquid 12 in 1 CASE LIQUID 12 1 59900-217-03 SoftenSure Antimicrobial Liquid 1200 mL in 1 BOTTLE LIQUID 1200 1 59900-217-04 SoftenSure Antimicrobial Liquid 4 in 1 CASE LIQUID 4 1 59900-217-04 SoftenSure Antimicrobial Liquid 1200 mL in 1 BOTTLE LIQUID 1200 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59900-217 SOFTENSURE ANTIMICROBIAL LIQUID (CHLOROXYLENOL) LIQUID [BEST SANITIZERS, INC] 1 Current NDC, 6 package rows 20241215_2929d297-4263-0d9a-e063-6294a90a762e.zip
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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 59900-217-01 59900021701 500 mL in 1 BOTTLE (59900-217-01) 500 ml 2023-12-26 No No Current 59900-217-02 59900021702 12 BOTTLE in 1 CASE (59900-217-02) / 500 mL in 1 BOTTLE 12 bottle 2023-12-26 No No Current 59900-217-03 59900021703 1200 mL in 1 BOTTLE (59900-217-03) 1200 ml 2023-12-26 No No Current 59900-217-04 59900021704 4 BOTTLE in 1 CASE (59900-217-04) / 1200 mL in 1 BOTTLE 4 bottle 2023-12-26 No No Current