Home NDC 70157-003-01 City Sunscreen serum Broad Spectrum SPF 30
Product NDC 70157-003
Requested package NDC 70157-003-01
11-digit product format 701570003
Labeler code 70157
Product ID 70157-003_efba9438-e3b8-86b4-e053-2995a90a2878
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octisalate, Avobenzene, Octocrylene
Dosage form CREAM
Route TOPICAL
Labeler Baxter Laboratories
Application M020
Marketing category OTC MONOGRAPH FINAL
Marketing start 2010-12-07
Marketing end 0000-00-00
Substance AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Active strength 3 g/100mL; g/100mL; g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record 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, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2022-08-30 03:57 UTC · source 2022-08-29 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 I Inactivated by FDA bd6a592717d7…303034d00443…2021-12-27 23:28 UTC · source 2021-12-27 I Inactivated by FDA 8dfbde2a14a4…c9ff85d89658…2020-12-18 03:04 UTC · source 2020-12-17 I Inactivated by FDA e2bbac7714bc…27bdfed8d636…2020-06-10 20:45 UTC · source 2020-06-10 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
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 70157-003-01 City Sunscreen serum Broad Spectrum SPF 30Supergoop 3 mL in 1 PACKET CREAM 3 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70157-003 CITY SUNSCREEN SERUM BROAD SPECTRUM SPF 30 SUPERGOOP (HOMOSALATE, OCTISALATE, AVOBENZENE, OCTOCRYLENE) CREAM [BAXTER LABORATORIES] 3 Legacy NDC, 1 package rows 20221217_51d5851a-4cc2-470e-97ba-5a40b201430f.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 44 of 354 · 7,077 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Abib Dewy tinted sunscreen Glow tube Light OCTISALATE, OCTOCRYLENE, ZINC OXIDE FOURCOMPANY CO., LTD. 4f165895-aa84-e215-e063-6394a90a6256 2026-04-10 Warnings Exact identifier application number: M020 Abib Dewy tinted sunscreen Glow tube Medium OCTISALATE, OCTOCRYLENE, ZINC OXIDE FOURCOMPANY CO., LTD. 4f16b8a4-4279-5f79-e063-6294a90a353d 2026-04-10 Warnings Exact identifier application number: M020 Sheer Touch Sunscreen SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE Amazon.com Services LLC f5ca0416-548c-4be0-a69e-c7e1b52aba95 2026-04-10 Warnings, Adverse reactions Exact identifier application number: M020 LASPA TINTED MATTE SUNSCREEN SPF 20 LIGHT ZINC OXIDE The Green Cricket Inc c56fd135-f46a-51ce-e053-2a95a90ab7b3 2026-04-10 Warnings Exact identifier application number: M020 CorTex SunX 50 Thick AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE CoreTex Products Inc f67a6c6c-c314-1c9d-e053-2a95a90a7f1a 2026-04-10 Warnings Exact identifier application number: M020 Nu Skin 180 Degree UV Block Hydrator SPF 18 OCTINOXATE AND ZINC OXIDE NSE Products, Inc. b9635e59-bb08-4167-b7ba-54c3fc712589 2026-04-09 Warnings Exact identifier application number: M020 Sport Sunscreen SPF 50 AVOBENZONE, HOMOSALATE, OCTISALATE The Kroger Co. 79c6fe2a-34c2-44cc-81bc-796c4463d2a6 2026-04-09 Warnings, Adverse reactions Exact identifier application number: M020 Arizona Sun ProductsSurfblok Lip Balm SPF 15 LIP BALM Arizona Sun Products 11fdbae5-84ec-7b1d-e063-6294a90a2878 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Prickly Pear Lip Balm SPF 15 SUNSCREEN LIP BALM Arizona Sun Products 11e9cb25-6ff8-a121-e063-6394a90a849e 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Sunscreen SPF 8 SUNSCREEN Arizona Sun Products 11e8b612-29be-47ed-e063-6394a90ab9e7 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun ProductsSurfblok Lip Balm SPF 15 LIP BALM Arizona Sun Products 11fdcfd0-8b24-7efc-e063-6294a90af7fa 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun SPF 45 Cycleblok Sunscreen SUNSCREEN Arizona Sun Products 11e71a84-12d1-2d4f-e063-6294a90adcd6 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun SPF 45 Bikerblok Sunscreen SUNSCREEN Arizona Sun Products 11e6eafd-f967-b748-e063-6394a90aabfd 2026-04-09 Warnings Exact identifier application number: M020 YSE Beauty Skin Glow Primer SPF 30 AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE MSS Beauty LLC 6a318e27-14e5-488e-ac19-010f69cb743d 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Sunscreen Kids Water Resistant SPF 30 SUNSCREEN Arizona Sun Products 116ed17c-3b38-5e96-e063-6294a90a4246 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun SPF 45 Surfblok Sunscreen SUNSCREEN Arizona Sun Products 11e76815-9316-555d-e063-6294a90aeb81 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Moisturizer SPF 3 MOISTURIZER Arizona Sun Products 1171af26-3040-552c-e063-6294a90ae220 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Sunscreen SPF15 SUNSCREEN Arizona Sun 10a600aa-4faa-47fc-e063-6294a90ac4ef 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Sunscreen Water Resistant SPF 30 SUNSCREEN Arizona Sun Products 11334e45-4bc2-d597-e063-6294a90a323e 2026-04-09 Warnings Exact identifier application number: M020 Arizona Sun Sunscreen Water Resistant SPF 30 SUNSCREEN Arizona Sun Products 1148e719-b8ed-11b3-e063-6394a90ac116 2026-04-09 Warnings Exact identifier application number: M020
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 70157-003-01 70157000301 3 mL in 1 PACKET (70157-003-01) 3 ml 2010-12-07 0000-00-00 No No Current