Home NDC 66077-693 INSTANT
Product NDC 66077-693
11-digit product format 660770693
Labeler code 66077
Product ID 66077-693_0c42240b-580d-eb4f-e063-6394a90a24ee
Type HUMAN OTC DRUG
Nonproprietary name INSTANT
Dosage form LIQUID
Route TOPICAL
Labeler Ultra-Chem, Inc.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-10-18
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
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 66077-693-01 INSTANT 118 mL in 1 BOTTLE, PLASTIC LIQUID 118 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 66077-693 INSTANT LIQUID [ULTRA-CHEM, INC.] 1 Current NDC, 1 package rows 20231213_0c425c6e-6c05-1748-e063-6394a90a9b5e.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 66077-693-01 66077069301 118 mL in 1 BOTTLE, PLASTIC (66077-693-01) 118 ml 2010-10-18 No No Current