Home NDC 78303-000-13 Apollo Instant Hand Sanitizer
Product NDC 78303-000
Requested package NDC 78303-000-13
11-digit product format 783030000
Labeler code 78303
Product ID 78303-000_aa684bea-80d2-e56c-e053-2995a90a24a4
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form GEL
Route TOPICAL
Labeler Sbu Group L.P. DBA Apollo Distributors
Application part333E
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-06-01
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 1 1/mL
NDC exclude flag No
Listing certified through 2021-12-31
Current FDA listing Historical FDA.report record 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 · 18 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 bd6a592717d7…303034d00443…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 78303-000-02 Apollo Instant Hand Sanitizer 60 mL in 1 BOTTLE GEL 60 2 78303-000-04 Apollo Instant Hand Sanitizer 120 mL in 1 BOTTLE GEL 120 2 78303-000-08 Apollo Instant Hand Sanitizer 237 mL in 1 BOTTLE GEL 237 2 78303-000-13 Apollo Instant Hand Sanitizer 5000 mL in 1 BOTTLE GEL 5000 2 78303-000-16 Apollo Instant Hand Sanitizer 500 mL in 1 BOTTLE GEL 500 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 78303-000 APOLLO INSTANT HAND SANITIZER (ALCOHOL) GEL [SBU GROUP L.P. DBA APOLLO DISTRIBUTORS] 2 Legacy NDC, 5 package rows 20200715_b4100cc4-1458-4a9c-8bb5-a5ad5d3372a3.zip
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 78303-000-13 78303000013 5000 mL in 1 BOTTLE (78303-000-13) 5000 ml 2020-06-01 0000-00-00 No No Current