Home NDC 42681-0010 Hand Sanitizer
Product NDC 42681-0010
11-digit product format 426810010
Labeler code 42681
Product ID 42681-0010_25f910c2-5ea8-ed23-e063-6394a90a1d5e
Type HUMAN OTC DRUG
Nonproprietary name Ethyl Alcohol
Dosage form GEL
Route TOPICAL
Labeler Whole Foods Market, Inc.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-01
Substance ALCOHOL
Active strength 62 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 · 28 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 42681-0010-2 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 42681-0010-2 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 42681-0010-2 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 42681-0010-2 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 42681-0010-2 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 42681-0010-2 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product D Discontinued by firm 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 42681-0010-2 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 42681-0010-2 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 42681-0010-2 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 42681-0010-1 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 42681-0010-1 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 42681-0010-1 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 42681-0010-1 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 42681-0010-1 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…
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 Hand Sanitizer
Brand name suffix Lavender
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 62 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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 581660 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 42681-0010-1 Hand SanitizerLavender 30 mL in 1 BOTTLE, PLASTIC GEL 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 42681-0010 HAND SANITIZER LAVENDER (ETHYL ALCOHOL) GEL [WHOLE FOODS MARKET, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20241104_ec8c7597-a3f1-65a8-e053-2995a90a69a1.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 45 of 115 · 2,286 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Biopure Antibacterial Hand Wipe Berry Strawberry BENZALKONIUM CHLORIDE Quest USA Corp 47d6574c-0d4c-392e-e063-6394a90a590f 2026-01-07 Warnings Exact identifier application number: M003 Biopure Antibacterial Hand Wipe Vallina Dream BENZALKONIUM CHLORIDE Quest USA Corp 47d7090d-036b-870b-e063-6394a90a80c3 2026-01-07 Warnings Exact identifier application number: M003 99 Plus Hand Sanitizer BENZEALKONIUM CHLORIDE Momar Incorporated f972a8f1-c928-4e4b-a8dd-a2fb77052d21 2026-01-06 Warnings Exact identifier application number: M003 Benzocaine BENZOCAINE Dynarex Corporation 6161e94c-7849-466e-8da3-a6f1b085bdf9 2026-01-06 Warnings Exact identifier application number: M003 Biopure Anti-bacterial Hand Wipes Fresh Morning Breeze Scent BENZALKONIUM CHLORIDE Quest USA Corp 47c105a8-7c76-9cde-e063-6294a90a9284 2026-01-06 Warnings Exact identifier application number: M003 SPA HAND SANITIZER VANILLA ETHYL ALCOHOL Rejoice International Corp. 47c3c187-da54-7c3b-e063-6294a90af3ce 2026-01-06 Warnings Exact identifier application number: M003 SPA HAND SANITIZER CHAMPAGNE BLASH ETHYL ALCOHOL Rejoice International Corp. 47c5e9af-4ea8-fb39-e063-6394a90aa5ab 2026-01-06 Warnings Exact identifier application number: M003 Antiseptic Cleaning wipe ANTISEPTIC CLEANING WIPE SHENZHEN BENLIJU BIO-TECH CO.,LTD 203d01ae-d99e-bce3-e063-6294a90a1a2d 2026-01-05 Warnings Exact identifier application number: M003 Povidone-lodine prep pad POVIDONE-LODINE PREP PAD SHENZHEN BENLIJU BIO-TECH CO.,LTD 201545b8-0697-5601-e063-6394a90a12f4 2026-01-05 Warnings Exact identifier application number: M003 Sting Relief prep Pad STING RELIEF PREP PAD SHENZHEN BENLIJU BIO-TECH CO.,LTD 202c7b77-1a48-52a5-e063-6394a90a2eb2 2026-01-05 Warnings Exact identifier application number: M003 Skin Cleaning Care Wipes SKIN CLEANING CARE WIPES SHENZHEN BENLIJU BIO-TECH CO.,LTD 203d7a95-65fe-ca65-e063-6294a90acc6e 2026-01-05 Warnings Exact identifier application number: M003 ANTISEPTIC CLEANSING WIPE(0.9% NACL) ANTISEPTIC CLEANSING WIPE(0.9% NACL) SHENZHEN BENLIJU BIO-TECH CO.,LTD 33e1c026-8a35-a47a-e063-6294a90a2406 2026-01-05 Warnings Exact identifier application number: M003 Hand Sanitizing Wipes HAND SANITIZING WIPES SHENZHEN BENLIJU BIO-TECH CO.,LTD 37487da6-4e0e-6625-e063-6394a90a0af1 2026-01-05 Warnings Exact identifier application number: M003 Hand wipes HAND WIPES SHENZHEN BENLIJU BIO-TECH CO.,LTD 39f3acca-7275-88ca-e063-6394a90ad1a2 2026-01-05 Warnings Exact identifier application number: M003 Smart Care Hand Sanitizer Vanilla Heaven ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 47a0781b-9b25-f04b-e063-6294a90ae7e5 2026-01-05 Warnings Exact identifier application number: M003 Smart Care Hand Sanitizer Berry ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 47a16397-dff3-7d79-e063-6394a90a040f 2026-01-05 Warnings Exact identifier application number: M003 IDOSWAB B ISOPROPYL ALCOHOL IDO PHARM 16d19630-b67a-f3e1-e063-6394a90a7429 2026-01-05 Warnings Exact identifier application number: M003 Sure Comfort Alcohol Prep Pads ISOPROPYL ALCOHOL IDO PHARM 27def94b-d3a6-18b7-e063-6394a90a22a6 2026-01-05 Warnings Exact identifier application number: M003 Smart Care Hand Sanitizer Lemon Lime ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 47aeaae9-740d-a28a-e063-6294a90a6460 2026-01-05 Warnings Exact identifier application number: M003 Smart Care Hand Sanitizer Calming Lavender ALCOHOL Shenzhen Lantern Scicence Co.,Ltd. 47aeeef9-0eed-e7d0-e063-6394a90a6d31 2026-01-05 Warnings Exact identifier application number: M003
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 42681-0010-1 42681001001 30 mL in 1 BOTTLE, PLASTIC (42681-0010-1) 30 ml 2024-11-03 0000-00-00 No No Current 42681-0010-2 42681001002 9 mL in 1 BOTTLE (42681-0010-2) 9 ml 2020-01-01 2024-12-31 No No Current