Home NDC 62032-909 Obagi Skintrinsiq Clarifiying Protocol
Product NDC 62032-909
11-digit product format 620320909
Labeler code 62032
Product ID 62032-909_a9c17c57-a3af-43d6-9db3-56fb8e28894b
Type HUMAN OTC DRUG
Nonproprietary name salicylic acid, titanium dioxide, and zinc oxide
Dosage form KIT
Labeler Obagi Cosmeceuticals LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-08-01
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 · 14 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 2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 62032-909-09 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 62032-909-09 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 62032-909-09 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 62032-909-09 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 62032-909-09 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 62032-909-09 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 62032-909-09 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 Obagi Skintrinsiq Clarifiying Protocol
Listing expiration 2026-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 251577 Internal RxNorm lookup 1235208 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 62032-612-04 Obagi Skintrinsiq Clarifiying Protocol 148 mL in 1 BOTTLE, PLASTIC LIQUID 148 mL 20 mg in 1mL 3 62032-811-09 Obagi Skintrinsiq Clarifiying Protocol 1 in 1 CARTON LOTION 15.6 g in 100g 3 62032-811-09 Obagi Skintrinsiq Clarifiying Protocol 85 g in 1 TUBE LOTION 85 g 15.6 g in 100g 3 62032-909-09 Obagi Skintrinsiq Clarifiying Protocol 1 in 1 BOX KIT 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62032-909 OBAGI SKINTRINSIQ CLARIFIYING PROTOCOL (SALICYLIC ACID, TITANIUM DIOXIDE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC] 3 Current NDC, Legacy NDC, 4 package rows 20250406_08ba9ea8-73fd-472b-9cc4-67df167352ec.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 52 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Lancome Paris UV Expert Aquagel Defense 50 Plus Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE AND OCTOCRYLENE L'Oreal USA Products Inc c500e58f-38b0-454e-8923-912844276b17 2026-03-20 Warnings Exact identifier application number: M020 Protect by HEALTHY SKIN LAB MD SUNSCREEN TINTED MOISTURIZER TITANIUM DIOXIDE, ZINC OXIDE HEALTHY SKIN LAB LIMITED 4a1ec566-549f-45f2-a43d-dacfc7263361 2026-03-20 Warnings Exact identifier application number: M020 SOJO sunscreen ZINC OXIDE Guangdong Aimu Biological Technology Co., Ltd 4d44efb6-abc5-c346-e063-6394a90a6023 2026-03-19 Warnings Exact identifier application number: M020 VRC Lip balm SPF15 ZINC OXIDE Guangdong Aimu Biological Technology Co., Ltd 4d588fbe-e61a-2264-e063-6394a90aa060 2026-03-19 Warnings Exact identifier application number: M020 SOjO Lip balm SPF15 ZINC OXIDE Guangdong Aimu Biological Technology Co., Ltd 4d5ed865-fff2-ee44-e063-6294a90a67e2 2026-03-19 Warnings Exact identifier application number: M020 ActivDerm Radiant Shield Broad Spectrum SPF 40 ZINC OXIDE ACTIVDERM LLC 4d6307f1-bab6-5f44-e063-6294a90a8e36 2026-03-19 Warnings Exact identifier application number: M020 Mad Robbit DEFEND SPF30 SUNSCREEN MAD RABBIT TATTOO, INC. bf853d54-ecd9-40cc-9f10-cb546bfb8933 2026-03-19 Warnings Exact identifier application number: M020 Stay Ageless Tinted Mineral Sunscreen BROAD SPECTRUM SPF30 SKNVcare, LLC 4d67dfb4-3607-2af6-e063-6294a90ae01a 2026-03-19 Warnings Exact identifier application number: M020 Premier Tinted Mineral Sunscreen BROAD SPECTRUM SPF30 Premier Plastic Surgery 4d3a36b9-7d60-01ac-e063-6294a90af4fb 2026-03-18 Warnings Exact identifier application number: M020 GOODAL HEARTLEAF SOOTHING ZINC 100 MINERAL SUNSCREEN ZINC OXIDE CLIO COSMETICS Co., Ltd. c7b13245-a3e0-4d53-b7fe-9b2c9707ab9e 2026-03-18 Warnings Exact identifier application number: M020 TIR TIR SUN BOUNCY GLOW LIP BALM SPF 30 BURNT MAPLE ZINC OXIDE COSMAX USA 4d318f51-1a43-44d5-e063-6394a90a4970 2026-03-17 Warnings Exact identifier application number: M020 TIR TIR SUN BOUNCY GLOW LIP BALM SPF 30 HAZY MAUVE ZINC OXIDE COSMAX USA 4d319110-e6a4-1ad3-e063-6394a90aa99c 2026-03-17 Warnings Exact identifier application number: M020 TIR TIR SUN BOUNCY GLOW LIP BALM SPF 30 SUNLIT CORAL ZINC OXIDE COSMAX USA 4d31b201-9d6a-730a-e063-6394a90a6700 2026-03-17 Warnings Exact identifier application number: M020 OSKIN New York Coffee BB Cream SPF 30 TITANIUM DIOXIDE, OCTOCRYLENE, ZINC OXIDE O'Skin Studio NY 29dae75a-4368-432a-9cf8-f0f021f09e29 2026-03-17 Warnings Exact identifier application number: M020 Premier Tinted Mineral Sunscreen BROAD SPECTRUM SPF30 Premier Plastic Surgery 4d39b64c-2e27-afed-e063-6394a90a3812 2026-03-17 Warnings Exact identifier application number: M020 Powder TITANIUM DIOXIDE Oxygen Development LLC 4d39ed7a-ca80-893c-e063-6294a90a03e7 2026-03-17 Warnings Exact identifier application number: M020 Powder TITANIUM DIOXIDE Oxygen Development LLC 4d3a0a92-b0de-a1ea-e063-6294a90a8508 2026-03-17 Warnings Exact identifier application number: M020 Avobenzone, Homosalate, Octisalate, Octocrylene AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Trader Joe's Company 4d3a36b9-7d63-01ac-e063-6294a90af4fb 2026-03-17 Warnings, Adverse reactions Exact identifier application number: M020 Redneck SPF 50 Sunscreen AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE Redneck Sunscreen LLC 4d3a460b-1b98-2906-e063-6294a90a3669 2026-03-17 Warnings Exact identifier application number: M020 Sunscreen BROAD SPECTRUM SPF 30 SKNVCARE, LLC 4d3ad051-3729-06fd-e063-6394a90ad0fe 2026-03-17 Warnings Exact identifier application number: M020
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 62032-612-04 62032061204 148 mL in 1 BOTTLE, PLASTIC 148 ml Historical 62032-811-09 62032081109 1 in 1 CARTON Historical 62032-909-09 62032090909 1 KIT in 1 BOX (62032-909-09) * 148 mL in 1 BOTTLE, PLASTIC (62032-612-04) * 1 BOTTLE, PUMP in 1 CARTON / 48 g in 1 BOTTLE, PUMP * 1 TUBE in 1 CARTON (62032-811-09) / 85 g in 1 TUBE * 59 mL in 1 BOTTLE, PLASTIC * 60 mL in 1 BOTTLE, PLASTIC 1 kit 2021-08-01 0000-00-00 No No Current