Home NDC 67879-104 PHARMA CLEAR SPOT TREATMENT
Product NDC 67879-104
11-digit product format 678790104
Labeler code 67879
Product ID 67879-104_4b359ce3-d2be-76bc-e063-6394a90ad075
Type HUMAN OTC DRUG
Nonproprietary name SALICYLIC ACID
Dosage form LIQUID
Route TOPICAL
Labeler PHARMAGEL INTERNATIONAL INC
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-06-15
Substance SALICYLIC ACID
Active strength 2 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 · 22 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 67879-104-51 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 67879-104-51 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 67879-104-51 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 67879-104-51 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 67879-104-51 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 67879-104-51 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 67879-104-51 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 67879-104-51 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 67879-104-51 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 67879-104-51 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 67879-104-51 367a005e9d99…383a685ebd0f…
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 PHARMA CLEAR SPOT TREATMENT
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 2 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 251577 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67879-104-11 PHARMA CLEAR SPOT TREATMENT 15 mL in 1 TUBE LIQUID 15 8 67879-104-51 PHARMA CLEAR SPOT TREATMENT 1 in 1 BOX LIQUID 1 8
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 3 of 55 · 1,088 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Acne Free Free 24 HR Acne Clearing System BENZOYL PEROXIDE AcneFree, LLC c939847a-72eb-96fa-e053-2a95a90a4f9c 2026-07-31 Warnings Exact identifier application number: M006 Terminator 10 BENZOYL PEROXIDE AcneFree, LLC c06778b6-0ed6-7d82-e053-2a95a90a2ef8 2026-07-31 Warnings Exact identifier application number: M006 Acne Free Oil Free Acne Cleanser 2.5 Benzoyl Peroxide BENZOYL PEROXIDE AcneFree LLC c939847a-72cc-96fa-e053-2a95a90a4f9c 2026-07-31 Warnings Exact identifier application number: M006 Benzoyl Peroxide Deep Cleansing Foaming Wash BENZOYL PEROXIDE AcneFree, LLC fe2d0e24-8c68-b2ea-e053-6294a90ad72c 2026-07-31 Warnings Exact identifier application number: M006 Salicylic Acid SALICYLIC ACID Acne Free, LLC 1097fc73-fa47-0f14-e063-6294a90aa499 2026-07-31 Warnings Exact identifier application number: M006 Even and Clear Cleanser SALICYLIC ACID Ambi Enterprises LLC bff537cf-aa79-5250-e053-2995a90a388a 2026-07-31 Warnings Exact identifier application number: M006 Oil Free Deep Cleansing Duo Cleansing Brush Oil Free Acne Cleanser BENZOYL PEROXIDE AcneFree, LLC c7a675fa-b6c0-6237-e053-2a95a90a0406 2026-07-31 Warnings Exact identifier application number: M006 Acne Free SEVERE ACNE 24 HR Acne Clearing System BENZOYL PEROXIDE AcneFree, LLC c939681e-ea93-31ce-e053-2a95a90a8c70 2026-07-31 Warnings Exact identifier application number: M006 Acne Free SENSITIVE SKIN 24 HR Acne Clearing System SALICYLIC ACID, BENZOYL PEROXIDE AcneFree LLC c9397a25-8fed-48d0-e053-2a95a90ab495 2026-07-31 Warnings Exact identifier application number: M006 sulfur acne treatment SULFUR Acne Free 105545d8-974c-5a9a-e063-6294a90aecc4 2026-07-31 Warnings Exact identifier application number: M006 24 Hour Sensitive Skin Acne Clearing System SALICYLIC ACID Acne Free LLC 39ea674d-ff6e-a8c6-e063-6394a90a0656 2026-07-31 Warnings Exact identifier application number: M006 cardae FOLLICULITIS Cream MICONAZOLE NITRATE 2% FOLLICULITIS CREAM Wenzhou Yuyuan Pharmaceutical Co., Ltd. 57e0be6a-3141-f3b6-e063-6394a90a1520 2026-07-30 Warnings Exact identifier application number: M006 SKINTIFIC 3X ACID INTENSIVE ACNE TREATMENT SALICYLIC ACID Gold Inti Trade Corporation 57a7c929-31f5-ef82-e063-6394a90ab9af 2026-07-28 Warnings Exact identifier application number: M006 Acne Treatment with Sulfur SULFUR DLC Laboratories, Inc. 4a1591e8-6135-4b22-b54c-5553c2dc0540 2026-07-28 Warnings Exact identifier application number: M006 amberglow BLEMISH PATCHES SALICYLIC ACID Pearl World Inc. 12054430-25ff-4b72-8f64-822b27abb443 2026-07-27 Warnings Exact identifier application number: M006 RFA BPO Acne Treatment 2.5% BENZOYL PEROXIDE Topiderm, Inc. c5053e9e-7608-45d9-9b9b-9b93210eb917 2026-07-27 Warnings Exact identifier application number: M006 ACNO Solution ACNE TREATMENT SALICYLIC ACID Noon Aesthetics M.R. Ltd 4a267e44-03d9-471f-9708-a5c60ff69097 2026-07-24 Warnings Exact identifier application number: M006 DERMFREE MILIA REMOVER SALICYLIC ACID 1% MILIA REMOVER Jiangxi Yudexi Pharmaceutical Co., LTD 4a5c8a6e-b02d-3a87-e063-6294a90a14ff 2026-07-23 Warnings Exact identifier application number: M006 salicylic acid SALICYLIC ACID Chain Drug Marketing Association 4dc96074-50a1-baa8-e063-6294a90a5aab 2026-07-22 Warnings, Adverse reactions Exact identifier application number: M006 SYLVIRENE MILIA REMOVER SALICYLIC ACID 1% MILIA REMOVER Jiangxi Yudexi Pharmaceutical Co., LTD 4a3751f8-2365-1b34-e063-6394a90acf74 2026-07-21 Warnings Exact identifier application number: M006
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 67879-104-11 67879010411 15 mL in 1 TUBE 15 ml Historical 67879-104-51 67879010451 1 TUBE in 1 BOX (67879-104-51) / 15 mL in 1 TUBE (67879-104-11) 1 tube 2016-06-15 0000-00-00 No No Current