Home NDC 21749-982 NDC 21749-982 - PURELL Advanced Foam Hand Rub 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 21749-982
Package NDCs from labels 21749-982-45, 21749-982-53, 21749-982-97, 21749-982-89, 21749-982-17
Manufacturer GOJO Industries, Inc.
Effective date 2024-12-31
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type PURELL Advanced Foam Hand Rub GOJO Industries, Inc. 2024-12-31 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 21749-982-17 PURELL Advanced Foam Hand Rub 515 mL in 1 PACKAGE LIQUID 515 3 21749-982-45 PURELL Advanced Foam Hand Rub 45 mL in 1 PACKAGE LIQUID 45 3 21749-982-53 PURELL Advanced Foam Hand Rub 535 mL in 1 PACKAGE LIQUID 535 3 21749-982-89 PURELL Advanced Foam Hand Rub 1200 mL in 1 PACKAGE LIQUID 1200 3 21749-982-97 PURELL Advanced Foam Hand Rub 700 mL in 1 PACKAGE LIQUID 700 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 21749-982 PURELL ADVANCED FOAM HAND RUB (ALCOHOL) LIQUID [GOJO INDUSTRIES, INC.] 3 5 package rows 20250101_f67dac52-88d9-4d46-84db-517b01acdcd9.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 21 of 196 · 3,903 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.