Home NDC 37808-809 inControl alcohol
Product NDC 37808-809
11-digit product format 378080809
Labeler code 37808
Product ID 37808-809_59568b8e-d818-2183-e063-6294a90a6100
Type HUMAN OTC DRUG
Nonproprietary name Isopropyl Alcohol
Dosage form SWAB
Route TOPICAL
Labeler H-E-B
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2010-11-01
Substance ISOPROPYL ALCOHOL
Active strength 70 mL/100mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2020-12-18 03:04 UTC · source 2020-12-17 excluded product product e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 37808-809-30 e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 37808-809-30 9bebd1f3094a…5416666fcb17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base inControl alcohol
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ISOPROPYL ALCOHOL 70 mL/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ND2M416302 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 797544 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37808-809-09 inControl alcohol 5 mL in 1 APPLICATOR SWAB 5 8 37808-809-09 inControl alcohol 1 in 1 PACKET SWAB 1 8 37808-809-30 inControl alcohol 100 in 1 BOX SWAB 100 8 37808-809-30 inControl alcohol 1 in 1 PACKET SWAB 1 8 37808-809-60 inControl alcohol 1 in 1 PACKET SWAB 1 8 37808-809-60 inControl alcohol 200 in 1 BOX SWAB 200 8
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-809 INCONTROL ALCOHOL (ISOPROPYL ALCOHOL) SWAB [H-E-B] 8 Current NDC, Legacy NDC, 6 package rows 20250105_45dfbd7a-0ae1-4146-9527-5483c884e636.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 100 of 115 · 2,286 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 37808-809-09 37808080909 1 APPLICATOR in 1 PACKET (37808-809-09) / 5 mL in 1 APPLICATOR 1 applicator 2010-11-01 0000-00-00 No No Current 37808-809-30 37808080930 100 PACKET in 1 BOX (37808-809-30) / 1 APPLICATOR in 1 PACKET / 5 mL in 1 APPLICATOR 100 packet 2010-11-01 0000-00-00 No No Current 37808-809-60 37808080960 200 PACKET in 1 BOX (37808-809-60) > 1 APPLICATOR in 1 PACKET (37808-809-09) > 5 mL in 1 APPLICATOR 200 packet 2010-11-01 0000-00-00 No No Current