Home NDC 69103-5500 Isopropyl Alcohol
Product NDC 69103-5500
11-digit product format 691035500
Labeler code 69103
Product ID 69103-5500_13a3cf2a-ee3b-be81-e063-6294a90a2981
Type HUMAN OTC DRUG
Nonproprietary name Isopropyl Alcohol
Dosage form SPRAY
Route TOPICAL
Labeler Provision Medical
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-07-25
Substance ISOPROPYL ALCOHOL
Active strength 700 mL/L
NDC exclude flag No
Listing certified through 2026-12-31
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 69103-5500 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 69103-5500 69103-5500-0 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Isopropyl Alcohol
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ISOPROPYL ALCOHOL 700 mL/L
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 1014638 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69103-5500-0 Isopropyl Alcohol 0.0591 L in 1 BOTTLE, SPRAY SPRAY 0.0591 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69103-5500 ISOPROPYL ALCOHOL SPRAY [PROVISION MEDICAL] 2 Current NDC, Legacy NDC, 1 package rows 20240322_ad045374-f4ad-4003-b350-8a2b0cbccb2e.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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 69103-5500-0 69103550000 .0591 L in 1 BOTTLE, SPRAY (69103-5500-0) 2022-07-25 0000-00-00 No No Current