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 138 of 353 · 7,049 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SHADED TITANIUM DIOXIDE, ZINC OXIDE Potency No. 710 LLC 3117e138-83a1-0931-e063-6394a90abe43 2025-12-10 Warnings Exact identifier application number: M020 SHADED TITANIUM DIOXIDE, ZINC OXIDE Potency No. 710 LLC 31188175-a4ca-449f-e063-6394a90a3c05 2025-12-10 Warnings Exact identifier application number: M020 COVERED ZINC OXIDE Potency No. 710 LLC 3118c3ed-f0f0-f997-e063-6294a90a53a9 2025-12-10 Warnings Exact identifier application number: M020 COVERED ZINC OXIDE Potency No. 710 LLC 3117faeb-1792-1b2e-e063-6294a90a92df 2025-12-10 Warnings Exact identifier application number: M020 Non-Tinted Mineral Foaming Sunscreen TITANIUM DIOXIDE, ZINC OXIDE Restore Skin Therapy, LLC 364b6af2-a0ed-4a17-e063-6394a90a3a17 2025-12-10 Exact identifier application number: M020 Morning Replenish ZINC OXIDE Restore Skin Therapy, LLC 364b26c2-a1bb-9660-e063-6294a90a14d1 2025-12-10 Exact identifier application number: M020 Glass Skin Sunscreen Tinted ZINC OXIDE Fleur de Lune, LLC 34288989-35b8-3aa3-e063-6394a90ac2c4 2025-12-10 Exact identifier application number: M020 Glass Skin Sunscreen Tinted ZINC OXIDE Fleur de Lune, LLC 3418394b-fede-65ce-e063-6394a90ad5f9 2025-12-10 Exact identifier application number: M020 Glass Skin Sunscreen Non-Tinted ZINC OXIDE Fleur de Lune, LLC 341871e5-c170-7560-e063-6394a90a8eee 2025-12-10 Exact identifier application number: M020 Glass Skin Sunscreen Non-Tinted ZINC OXIDE Fleur de Lune, LLC 3428bdbb-1f18-a29b-e063-6294a90addbc 2025-12-10 Exact identifier application number: M020 Sheer Facial Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE BB MEDICAL & DERMATOLOGY INC 342b2403-4f4a-3e77-e063-6294a90a4f0a 2025-12-10 Exact identifier application number: M020 Sheer Mineral Sunscreen Bar TITANIUM DIOXIDE, ZINC OXIDE BB MEDICAL & DERMATOLOGY INC 342b69d5-f0e1-99cd-e063-6294a90abb6e 2025-12-10 Exact identifier application number: M020 Sheer Facial Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE BB MEDICAL & DERMATOLOGY INC 342c3f42-c17f-f777-e063-6394a90a8058 2025-12-10 Exact identifier application number: M020 Lip SPF TITANIUM DIOXIDE, ZINC OXIDE FRANCISCO FLORES, M.D., P.A. 396d3fdd-99d8-77e8-e063-6294a90aec2f 2025-12-10 Exact identifier application number: M020 Non-Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE FRANCISCO FLORES, M.D., P.A. 396cae82-7641-e1b2-e063-6394a90a7c07 2025-12-10 Exact identifier application number: M020 Solar Knight SPF 40 Broad Spectrum TITANIUM DIOXIDE, ZINC OXIDE MASCARENAS ENTERPRISES, INC. 36c27c91-22ac-205c-e063-6294a90ab379 2025-12-10 Exact identifier application number: M020 Tinted Mineral Sunscreen TITANIUM DIOXIDE, ZINC OXIDE FRANCISCO FLORES, M.D., P.A. 396ce15a-06ad-4055-e063-6294a90a27fb 2025-12-10 Exact identifier application number: M020 Dermablue Daily Replenishing ZINC OXIDE Dermablue, P.C. 308da9c9-544e-d5d1-e063-6294a90aa49b 2025-12-10 Warnings Exact identifier application number: M020 Recoverie Mineral Matte ZINC OXIDE Clear Day Acne Clinic 308f41de-fb14-40f9-e063-6394a90a008f 2025-12-10 Warnings Exact identifier application number: M020 AL0043600 Alba Botanica VE Herbal Healing Body COLLOIDAL OATMEAL The Hain Celestial Group, Inc. 60672feb-141f-651e-e053-2a91aa0af41d 2025-12-10 Warnings 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