Home NDC 79306-010-10 COLLOID 5010 S
Product NDC 79306-010
Requested package NDC 79306-010-10
11-digit product format 793060010
Labeler code 79306
Product ID 79306-010_aafd4977-394e-2666-e053-2a95a90a6f78
Type HUMAN OTC DRUG
Nonproprietary name ALCOHOL
Dosage form LIQUID
Route TOPICAL
Labeler COLLOIDS DE MEXICO, S.A. DE C.V.
Application part333A
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2020-05-05
Marketing end 0000-00-00
Substance ALCOHOL
Active strength 80 mL/100mL
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 79306-010-11 COLLOID 5010 S 1000 mL in 1 BOTTLE, PLASTIC LIQUID 1000 2 79306-010-10 COLLOID 5010 S 3780 mL in 1 BOTTLE, PLASTIC LIQUID 3780 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 79306-010 COLLOID 5010 S (ALCOHOL) LIQUID [COLLOIDS DE MEXICO, S.A. DE C.V.] 2 Legacy NDC, 1 package rows 20200722_aaf78cc1-1536-fa4b-e053-2995a90aa3c8.zip 79306-010 COLLOID 5010 S (ALCOHOL) LIQUID [COLLOIDS DE MEXICO, S.A. DE C.V.] 1 Legacy NDC, 1 package rows 20200718_aaa909de-f87d-22af-e053-2a95a90ae8c2.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 79306-010-10 79306001010 3780 mL in 1 BOTTLE, PLASTIC (79306-010-10) 3780 ml 2020-05-05 0000-00-00 No No Current