Home NDC 72104-926 CB Multi-Active Moisturizer with SPF 30
Product NDC 72104-926
11-digit product format 721040926
Labeler code 72104
Product ID 72104-926_ff4db85b-f966-42b2-8190-5f05f4ae7649
Type HUMAN OTC DRUG
Nonproprietary name Octinoxate, Homosalate, Octisalate, Oxybenzone and Avobenzone
Dosage form CREAM
Route TOPICAL
Labeler Innovation Brands Inc.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-06-30
Substance OCTINOXATE; HOMOSALATE; OCTISALATE; OXYBENZONE; AVOBENZONE
Active strength 7.4; 6.2; 5; 3.1; 1.5 g/100g; g/100g; g/100g; g/100g; g/100g
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 72104-926-89 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 72104-926-89 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 72104-926-89 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 72104-926-89 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 72104-926-89 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 72104-926-89 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 72104-926-89 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 CB Multi-Active Moisturizer with SPF 30
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTINOXATE 7.4 g/100g HOMOSALATE 6.2 g/100g OCTISALATE 5 g/100g OXYBENZONE 3.1 g/100g AVOBENZONE 1.5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72104-926-89 CB Multi-Active Moisturizer with SPF 30 1 in 1 CARTON CREAM 1 2 72104-926-89 CB Multi-Active Moisturizer with SPF 30 50 g in 1 JAR CREAM 50 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72104-926 CB MULTI-ACTIVE MOISTURIZER WITH SPF 30 (OCTINOXATE, HOMOSALATE, OCTISALATE, OXYBENZONE AND AVOBENZONE) CREAM [LIONESSE USA, INC.] 1 Current NDC, 2 package rows 20230707_d9557a6c-78e9-4b01-8a4b-e0eceb511c4e.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 135 of 353 · 7,049 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SUNerchi Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE SYNERCHI MED SPA, INC. 37db5721-2b32-d4d8-e063-6294a90a47d7 2025-12-11 Exact identifier application number: M020 SUNerchi Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE SYNERCHI MED SPA, INC. 37db14e1-f995-b649-e063-6294a90afd69 2025-12-11 Exact identifier application number: M020 208 ZINC OXIDE PETER L. KOPELSON, M.D. 351ce033-6bd0-574e-e063-6394a90af448 2025-12-11 Exact identifier application number: M020 208 ZINC OXIDE PETER L. KOPELSON, M.D., 351c9727-d7ac-9c3f-e063-6294a90a7721 2025-12-11 Exact identifier application number: M020 Replenishing Daily Protection Tinted ZINC OXIDE MY FAVORITE PLACE SPA LLC 351c0c1e-5712-1e23-e063-6394a90abe6f 2025-12-11 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Saving Face Skinspa Inc. 351d27e3-00d4-8d31-e063-6394a90aaf72 2025-12-11 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Saving Face Skinspa Inc. 351db99e-262f-b67e-e063-6394a90a3418 2025-12-11 Exact identifier application number: M020 Replenishing Daily Protection NT ZINC OXIDE MY FAVORITE PLACE SPA LLC 351c5f6f-86e6-7219-e063-6294a90a3745 2025-12-11 Exact identifier application number: M020 Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE DAISY'S SKIN TRANSFORMATION LLC 37d9fbf5-d602-d3dc-e063-6394a90abe53 2025-12-11 Exact identifier application number: M020 Tinted Mineral 40 TITANIUM DIOXIDE, ZINC OXIDE 2301 PLASTIC SURGERY, PLLC 374d53a7-be0b-4d7a-e063-6394a90a37c4 2025-12-11 Exact identifier application number: M020 Daily Protection 40 ZINC OXIDE 2301 PLASTIC SURGERY, PLLC 374d9c77-ed9f-a518-e063-6394a90a34fa 2025-12-11 Exact identifier application number: M020 Tinted Mineral 40 TITANIUM DIOXIDE, ZINC OXIDE 2301 PLASTIC SURGERY, PLLC 374df66d-eb9b-c4a7-e063-6394a90a3cc6 2025-12-11 Exact identifier application number: M020 Daily Protection 40 ZINC OXIDE 2301 PLASTIC SURGERY, PLLC 374e2294-7281-c7b9-e063-6394a90acc89 2025-12-11 Exact identifier application number: M020 Facial Mineral Sunscreen Mineral Protection TITANIUM DIOXIDE, ZINC OXIDE CAPE COD SKIN CARE CO. INC. 387f6dd5-3901-0849-e063-6294a90af8bc 2025-12-11 Exact identifier application number: M020 Non - Tinted Mineral Sunscreen ZINC OXIDE NEXTEX CORPORATION 35bacfcf-0254-aa0a-e063-6394a90a1475 2025-12-11 Exact identifier application number: M020 Facial Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE LEDUC, XUANTO MD 387e2e59-c5db-c70e-e063-6394a90a2d26 2025-12-11 Exact identifier application number: M020 Facial Mineral Sunscreen Mineral Protection TITANIUM DIOXIDE, ZINC OXIDE CAPE COD SKIN CARE CO. INC. 390779a8-4556-27a5-e063-6294a90a1200 2025-12-11 Exact identifier application number: M020 non-tinted sheer matte mineral TITANIUM DIOXIDE, ZINC OXIDE NEXTEX CORPORATION 35ba6cc9-0d49-6d0c-e063-6394a90ac7c3 2025-12-11 Exact identifier application number: M020 sheer tinted matte mineral TITANIUM DIOXIDE, ZINC OXIDE NEXTEX CORPORATION 35ba9ca7-fe5c-9824-e063-6394a90a5c46 2025-12-11 Exact identifier application number: M020 illuminating mineral mousse TITANIUM DIOXIDE, ZINC OXIDE NEXTEX CORPORATION 35bb4d67-373f-f60c-e063-6394a90a974d 2025-12-11 Exact identifier application number: M020
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72104-926-89 72104092689 1 JAR in 1 CARTON (72104-926-89) / 50 g in 1 JAR 1 jar 2023-06-30 No No Current