Home NDC 71853-006-01 ElimiShield Home and Outdoor Moisturizing Hand Sanitizer
Product NDC 71853-006
Requested package NDC 71853-006-01
11-digit product format 718530006
Labeler code 71853
Product ID 71853-006_09c2d98f-43b9-301f-e063-6394a90aff3f
Type HUMAN OTC DRUG
Nonproprietary name BENZALKONIUM CHLORIDE
Dosage form LIQUID
Route TOPICAL
Labeler Bryson Industries Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-09-01
Substance BENZALKONIUM CHLORIDE
Active strength 1.3 mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base ElimiShield Home and Outdoor Moisturizing Hand Sanitizer
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZALKONIUM CHLORIDE 1.3 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F5UM2KM3W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1049254 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71853-006-01 ElimiShield Home and Outdoor Moisturizing Hand Sanitizer 50 mL in 1 BOTTLE LIQUID 50 2 71853-006-02 ElimiShield Home and Outdoor Moisturizing Hand Sanitizer 200 mL in 1 BOTTLE LIQUID 200 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71853-006 ELIMISHIELD HOME AND OUTDOOR MOISTURIZING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [BRYSON INDUSTRIES INC.] 2 Current NDC, Legacy NDC, 2 package rows 20231110_affeb47c-0e10-7f04-e053-2a95a90a4f1f.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71853-006-01 71853000601 50 mL in 1 BOTTLE (71853-006-01) 50 ml 2020-09-01 0000-00-00 No No Current