Home NDC 71141-849 Alcohol
Product NDC 71141-849
11-digit product format 711410849
Labeler code 71141
Product ID 71141-849_4a0570d1-7d24-9ac9-e063-6394a90a3742
Type HUMAN OTC DRUG
Nonproprietary name Alcohol
Dosage form LIQUID
Route TOPICAL
Labeler Lidl US, LLC
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-06-28
Substance ALCOHOL
Active strength 62 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Alcohol
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 62 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3K9958V90M Internal UNII 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 71141-849-34 Alcohol 236 mL in 1 BOTTLE, PLASTIC LIQUID 236 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71141-849 ALCOHOL LIQUID [LIDL US, LLC] 9 Current NDC, Legacy NDC, 1 package rows 20250515_c7746330-2943-491a-bafc-0c8dd4fa40e2.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 Marketing end Sample Exclude flag Status 71141-849-34 71141084934 236 mL in 1 BOTTLE, PLASTIC (71141-849-34) 236 ml 2021-06-28 0000-00-00 No No Current