Home NDC 0096-0721 Daily Facial Moisturizer
Product NDC 0096-0721
11-digit product format 000960721
Labeler code 0096
Product ID 0096-0721_4bac1be4-bde9-8a04-e063-6394a90a438e
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen
Dosage form CREAM
Route TOPICAL
Labeler Person and Covey
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 1991-08-01
Substance HOMOSALATE; AVOBENZONE; OCTINOXATE; OCTOCRYLENE
Active strength .06; .03; .075; .015 g/g; g/g; g/g; g/g
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 · 24 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 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 0096-0721-07 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 0096-0721-07 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 0096-0721-07 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 0096-0721-07 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 0096-0721-07 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 0096-0721-07 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 0096-0721-45 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 0096-0721-07 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 0096-0721-45 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 0096-0721-07 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 0096-0721-45 I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 0096-0721-07 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 excluded product product I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 0096-0721-45 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2021-12-27 23:28 UTC · source 2021-12-27 excluded package package 0096-0721-07 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 excluded product product I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 0096-0721-45 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 0096-0721-07 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 excluded product product I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 0096-0721-45 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 0096-0721-07 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…
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 Daily Facial Moisturizer
Brand name suffix SPF 25
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength HOMOSALATE .06 g/g AVOBENZONE .03 g/g OCTINOXATE .075 g/g OCTOCRYLENE .015 g/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 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 0096-0721-07 Daily Facial MoisturizerSPF 25 7 g in 1 BOTTLE CREAM 7 9 0096-0721-10 Daily Facial MoisturizerSPF 25 10 g in 1 TUBE CREAM 10 9 0096-0721-45 Daily Facial MoisturizerSPF 25 45 g in 1 BOTTLE CREAM 45 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0096-0721 DAILY FACIAL MOISTURIZER SPF 25 (SUNSCREEN) CREAM [PERSON AND COVEY] 5 Current NDC, Legacy NDC, 3 package rows 20250221_6b9258e4-c7c6-765e-e053-2991aa0a9f4e.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 23 of 357 · 7,139 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ultra Violette Preen Screen Broad Spectrum SPF 50 AVONBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE Grace and Fire USA Inc. 26a0fc0d-a903-2ac1-e063-6394a90a13db 2026-06-01 Warnings Exact identifier application number: M020 Timesavvy Hybrid XL Cushion Sun Serum SPF 50 HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE ProBetter USA, Inc. 82a22071-f1bd-4fab-b929-8a00ef18f0d9 2026-05-31 Warnings Exact identifier application number: M020 Marine Screen Mineral Sunscreen Broad Spectrum SPF 50 ZINC OXIDE OSEA International, LLC 9aa20377-0ab9-4205-b9aa-24640a4641e7 2026-05-29 Warnings Exact identifier application number: M020 Ciele Blush and Protect Sugar ZINC OXIDE Ciele LLC 52f3a9f6-a226-6723-e063-6394a90a8706 2026-05-29 Warnings Exact identifier application number: M020 KIEHLS DERMATOLOGIST SOLUTIONS BETTER SCREEN MINER ALL UV SERUM BROAD SPECTRUM SPF 50 PLUS MINERAL SUNSCREEN TITANIUM DIOXIDE AND ZINC OXIDE LOreal USA Products Inc 294e6049-12b5-4b45-ae00-8ee1d9d2a1a4 2026-05-29 Warnings Exact identifier application number: M020 Daily Mineral Sunscreen 20% Zinc Oxide ZINC OXIDE INTEGRATIVE AESTHETICS BOSTON, LLC 52f818f4-8485-b228-e063-6294a90a9fe3 2026-05-29 Warnings Exact identifier application number: M020 Dr.G BRIGHT TONING UP TINTED SUNSCREEN ZINC OXIDE, OCTISALATE, HOMOSALATE GOWOONSESANG COSMETICS CO., LTD. 30d34459-b7fb-b0c6-e063-6294a90a08ac 2026-05-28 Warnings Exact identifier application number: M020 Dr.G GREEN MILD UP DEFENSE MINERAL SUNSCREEN ZINC OXIDE GOWOONSESANG COSMETICS CO., LTD. 30d49f24-3e13-385f-e063-6294a90ab5c8 2026-05-28 Warnings Exact identifier application number: M020 Dr.G R.E.D BLEMISH SOOTHING UP MOISTURE SUNSCREEN HOMOSALATE, OCTISALATE, AVOBENZONE GOWOONSESANG COSMETICS CO., LTD. 30d53b8a-7e35-0b2b-e063-6294a90aa8df 2026-05-28 Warnings Exact identifier application number: M020 Ciele Blush and Protect Berri ZINC OXIDE Ciele LLC 52e16cbc-b452-db18-e063-6394a90a4081 2026-05-28 Warnings Exact identifier application number: M020 Ciele Blush and Protect June ZINC OXIDE Ciele LLC 52e1c504-f0ee-2853-e063-6394a90a3139 2026-05-28 Warnings Exact identifier application number: M020 Ciele Blush and Protect January ZINC OXIDE Ciele LLC 52e186df-06aa-6528-e063-6294a90a3888 2026-05-28 Warnings Exact identifier application number: M020 Ciele Blush and Protect Berri ZINC OXIDE Ciele LLC 52e1398d-b170-ea89-e063-6294a90a7d24 2026-05-28 Warnings Exact identifier application number: M020 TIZO ULTRA NON TINTED MINERAL SUNSCREEN ZINC OXIDE 20% Fallien Cosmeceuticals, LTD 30d30610-2e6c-418c-bbcf-4ecd7f61be93 2026-05-28 Warnings Exact identifier application number: M020 Creme Foundation ZINC OXIDE Lauren Brooke Cosmetiques LLC 4d09907e-ddcd-9d62-e063-6394a90acf3f 2026-05-28 Warnings Exact identifier application number: M020 GOONGBE Moisture Sun Cushion Mild SPF 50 ZINC OXIDE Zero to Seven Inc. 1e8720b4-5e8b-dc8b-e063-6394a90aad34 2026-05-27 Warnings Exact identifier application number: M020 GOONGBE Fresh Sun Stick Mild SPF 50 ZINC OXIDE Zero to Seven Inc. 1e8727a4-0dc0-19dc-e063-6394a90a82b6 2026-05-27 Warnings Exact identifier application number: M020 Tallow and Sol SUNSCREEN SPF30 NON-NANO ZINC OXIDE 20% Guangzhou Shengyanghui Industrial Trading Co., Ltd 52c9dc0a-41f7-3e8a-e063-6394a90a8fca 2026-05-27 Warnings Exact identifier application number: M020 Tallow and SolSUNSCREEN SPF50 NON-NANO ZINC OXIDE 25% Guangzhou Shengyanghui Industrial Trading Co., Ltd 52cb56cf-f092-9f86-e063-6394a90ac2d3 2026-05-27 Warnings Exact identifier application number: M020 SPF 50 Mineral Sunscreen Face and Body ZINC OXIDE Toddle Born Wild, Inc. e97d82fe-cd45-43a5-9c1f-3900025240a1 2026-05-27 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 0096-0721-07 00096072107 7 g in 1 BOTTLE 7 g Historical 0096-0721-10 00096072110 10 g in 1 TUBE (0096-0721-10) 10 g 2026-02-23 Yes No Current 0096-0721-45 00096072145 45 g in 1 BOTTLE (0096-0721-45) 45 g 1991-08-01 No No Current