Home NDC 69740-212-00 I.V. Prep Antiseptic Wipe
Product NDC 69740-212
Requested package NDC 69740-212-00
11-digit product format 697400212
Labeler code 69740
Product ID 69740-212_143483a1-294e-017e-e063-6294a90a0456
Type HUMAN OTC DRUG
Nonproprietary name ISOPROPYL ALCOHOL
Dosage form CLOTH
Route TOPICAL
Labeler Smith & Nephew, Medical Ltd
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 1999-10-01
Substance ISOPROPYL ALCOHOL
Active strength 70 mL/100mL
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 · 3 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 2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 69740-212 69740-212-00 I Inactivated by FDA excluded / ndc_excluded.zip 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 69740-212 69740-212-00 I Inactivated by FDA excluded / ndc_excluded.zip 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 69740-212 69740-212-00 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base I.V. Prep Antiseptic Wipe
Listing expiration 2026-12-31 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69740-212-00 I.V. Prep Antiseptic Wipe 50 in 1 BOX CLOTH 50 8 69740-212-00 I.V. Prep Antiseptic Wipe 3.7 mL in 1 POUCH CLOTH 3.7 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69740-212 I.V. PREP ANTISEPTIC WIPE (ISOPROPYL ALCOHOL) CLOTH [SMITH & NEPHEW, MEDICAL LTD] 8 Current NDC, Legacy NDC, 2 package rows 20240605_50f1c74a-bb8e-41c2-a7ee-f2d310a372a7.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 Units Marketing start Marketing end Sample Exclude flag Status 69740-212-00 69740021200 50 POUCH in 1 BOX (69740-212-00) / 3.7 mL in 1 POUCH 50 pouch 1999-10-01 0000-00-00 No No Current