Home NDC 69060-6930 INSTANT HAND SANITIZER
Product NDC 69060-6930
11-digit product format 690606930
Labeler code 69060
Product ID 69060-6930_249d509a-83c9-7e5b-e063-6394a90ad5f1
Type HUMAN OTC DRUG
Nonproprietary name INSTANT HAND SANITIZER
Dosage form LIQUID
Route TOPICAL
Labeler Rainbow Technology Corporation
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-05-24
Substance ALCOHOL
Active strength 67 mL/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base INSTANT HAND SANITIZER
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 67 mL/100mL
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 69060-6930-2 INSTANT HAND SANITIZER 236 mL in 1 BOTTLE, PLASTIC LIQUID 236 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69060-6930 INSTANT HAND SANITIZER LIQUID [RAINBOW TECHNOLOGY CORPORATION] 1 Current NDC, 1 package rows 20241019_249d50e1-da31-1975-e063-6294a90afc84.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 69060-6930-2 69060693002 236 mL in 1 BOTTLE, PLASTIC (69060-6930-2) 236 ml 2013-05-24 No No Current