Home NDC 72317-001-01 RosaAcne Relief
Product NDC 72317-001
Requested package NDC 72317-001-01
11-digit product format 723170001
Labeler code 72317
Product ID 72317-001_e9dd15ee-22bd-4bcd-b5ff-20cb9bf8a4af
Type HUMAN OTC DRUG
Nonproprietary name Sulfur, Salicylic Acid
Dosage form OINTMENT
Route TOPICAL
Labeler Kunming Zhongzhou Pharmaceutical Co, Ltd
Application part333D
Marketing category OTC MONOGRAPH FINAL
Marketing start 2018-07-18
Marketing end 0000-00-00
Substance SULFUR; SALICYLIC ACID
Active strength 7 g/100g; g/100g
NDC exclude flag No
Listing certified through 2020-12-31
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.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72317-001-01 RosaAcne Relief 1 in 1 BOX OINTMENT 1 32463 72317-001-01 RosaAcne Relief 20 g in 1 BOTTLE, PLASTIC OINTMENT 20 32463
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72317-001 ROSAACNE RELIEF (SULFUR, SALICYLIC ACID) OINTMENT [KUNMING ZHONGZHOU PHARMACEUTICAL CO, LTD] 32463 Legacy NDC, 2 package rows 20180731_2fda4df9-9449-4ded-b903-b93dd8efb19b.zip
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 72317-001-01 72317000101 1 BOTTLE, PLASTIC in 1 BOX (72317-001-01) > 20 g in 1 BOTTLE, PLASTIC 2018-07-18 0000-00-00 No No Current