Home NDC 70157-003 City Sunscreen serum Broad Spectrum SPF 30
Product NDC 70157-003
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 · 44 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 product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 70157-003-01 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 70157-003-01 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…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 70157-003-01 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 70157-003-01 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 70157-003-01 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 70157-003-01 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 70157-003-01 I Inactivated by FDA 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 70157-003-01 I Inactivated by FDA ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 70157-003-01 I Inactivated by FDA 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 70157-003-01 I Inactivated by FDA ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 70157-003-01 I Inactivated by FDA 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 70157-003-01 I Inactivated by FDA 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 excluded product product I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-28 21:12 UTC · source 2024-05-28 excluded package package 70157-003-01 I Inactivated by FDA 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 excluded product product I Inactivated by FDA 834df4deac94…adcc014656a3…2024-05-15 03:39 UTC · source 2024-05-14 excluded package package 70157-003-01 I Inactivated by FDA 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 excluded product product I Inactivated by FDA 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 70157-003-01 I Inactivated by FDA 1332a3947898…d4bfe170f9cd…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 70157-003-01 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 70157-003-01 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 70157-003-01 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 70157-003-01 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 70157-003-01 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 70157-003-01 I Inactivated by FDA 9bebd1f3094a…5416666fcb17…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 70157-003-01 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 254 of 346 · 6,912 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join MILK TINT SPF 43 TINTED PRIMER SERUM MEDIUM ZINC OXIDE COSMAX USA, CORPORATION 298707d4-72ed-796f-e063-6294a90aa5cd 2024-12-18 Warnings Exact identifier application number: M020 MILK TINT SPF 43 TINTED PRIMER SERUM LIGHT ZINC OXIDE COSMAX USA, CORPORATION 29871c02-9adf-6266-e063-6394a90a20ab 2024-12-18 Warnings Exact identifier application number: M020 MILK TINT SPF 43 TINTED PRIMER SERUM TAN ZINC OXIDE COSMAX USA, CORPORATION 29874029-24bf-b2ce-e063-6394a90acd4d 2024-12-18 Warnings Exact identifier application number: M020 Babo Botanicals Sheer Zinc Mineral Sunscreen SPF 30 ZINC OXIDE Babo Botanicals, Inc. 2990e4ff-5bdb-3008-e063-6294a90a9497 2024-12-18 Warnings Exact identifier application number: M020 Tinted Lip Cream SPF 15 ZINC OXIDE COSMAX USA, CORPORATION 29915354-4673-7444-e063-6294a90a0fd1 2024-12-18 Warnings Exact identifier application number: M020 Mineral Lip Balm SPF-15 ZINC OXIDE TUBBY TODD 4d938672-5302-4e47-a582-c3e6467008cb 2024-12-18 Warnings Exact identifier application number: M020 SaltyFace Daily Sun Shield Mineral Sunscreen For Face SPF 30 ZINC OXIDE Saltyface Natural Inc f0cc7ce9-81b3-439f-b5ee-96138de54e78 2024-12-18 Warnings Exact identifier application number: M020 Belasol Suncream Non Tinted Moisturizing Sunscreen SPF 50 Jasmine TITANIUM DIOXIDE, ZINC OXIDE EK Clothing LLC dba Belasol e999d752-6c00-459e-b6c3-d264c330597d 2024-12-18 Warnings Exact identifier application number: M020 Belasol Suncream Non Tinted Moisturizing Sunscreen SPF 50 TITANIUM DIOXIDE, ZINC OXIDE EK Clothing LLC dba Belasol f22626c1-0996-41d8-a2ec-3bf7491df657 2024-12-18 Warnings Exact identifier application number: M020 Costa Sea Mineral Sunscreen SPF 50 ZINC OXIDE COSTA SEA INC 841e1b3d-dbbc-4bb0-886a-fb2d077ae739 2024-12-18 Warnings Exact identifier application number: M020 SPF 50 plus Sunscreen All Mineral Active Ingredients TITANIUM DIOXIDE AND ZINC OXIDE KAS Direct LLC dba BabyGanics 247aae3d-1845-4dd8-b774-b9e8214809a2 2024-12-18 Warnings Exact identifier application number: M020 Softlips Vanilla, Watermelon, Cherry DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE The Mentholatum Company 2235d029-157e-4a30-be90-605e6bc143fd 2024-12-17 Warnings Exact identifier application number: M020 Softlips Salted Caramel, Candy Apple, Marshmallow Ghost DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE The Mentholatum Company 42cf4623-0eb8-455a-b374-8e17e9336b92 2024-12-17 Warnings Exact identifier application number: M020 Softlips Peppermint Mocha, Apple Chai Cider, Orange Cranberry DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE The Mentholatum Company 0338c078-695d-4d4e-9e90-5a8a98d49524 2024-12-17 Warnings Exact identifier application number: M020 Softlips Pearl Plus Vanilla DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE The Mentholatum Company 107bcaa9-4347-4979-be44-35183a9ee67e 2024-12-17 Warnings Exact identifier application number: M020 Softlips Raspberry DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE The Mentholatum Company d18b4c19-0365-44ec-bea8-4328e537e0d8 2024-12-17 Warnings Exact identifier application number: M020 Softlips Watermelon DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE The Mentholatum Company 03062f13-270d-49cf-8939-2349f12e9cba 2024-12-17 Warnings Exact identifier application number: M020 Softlips Vanilla Watermelon DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE The Mentholatum Company f733747a-ad1a-4222-baf1-69dcd90a3350 2024-12-17 Warnings Exact identifier application number: M020 Softlips Vanilla Watermelon DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE The Mentholatum Company 1fbe85a2-4cd7-45bd-85a2-83bbf75c5f97 2024-12-17 Warnings Exact identifier application number: M020 Softlips Marshmallow Ghost DIMETHICONE, OCTINOXATE, OCTISALATE, OXYBENZONE The Mentholatum Company 8d55141d-5d6f-4eec-87dc-d3c808cf7a6a 2024-12-17 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