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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	70157-003		I	Inactivated by FDA		2026-10-16
excluded package	package	70157-003	70157-003-01	I	Inactivated by FDA		2026-10-16

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#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029
444b3e50-f226-46ef-bfca-2e7035d140cd	Product name	1	20190611
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
597b1cfd-7b31-5048-62be-ca5cd740da2f	Product name	1	20140508
ec2149b3-5c6d-5344-f757-c86411073075	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70157-003-01	2024-01-30	C162847	48780-1	9d75b9d1-26a0-f424-e053-dadaa90a57ce	City Sunscreen Serum Broad Spectrum SPF 30
70157-003-01	2022-12-02	C162847	48780-1	9d75b9d1-26a0-f424-e053-dadaa90a57ce	City Sunscreen Serum Broad Spectrum SPF 30
70157-003-01	2020-01-31	C162847	48780-1	9d75b9d1-26a0-f424-e053-dadaa90a57ce	City Sunscreen Serum Broad Spectrum SPF 30

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 85 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
100% Mineral Broad Spectrum Sunscreen SPF 50	TITANIUM DIOXIDE, ZINC OXIDE	Supergoop LLC	d6fcc065-cbcd-0b81-e053-2a95a90ab1f9	2026-01-09	Warnings	Exact identifier application number: M020
Glow Screen Body Broad Spectrum Sunscreen SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	b9590938-417d-617a-e053-2995a90a7496	2026-01-09	Warnings	Exact identifier application number: M020
100% Mineral Broad Spectrum Sunscreen SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Supergoop LLC	d7758651-c152-5868-e053-2a95a90ab673	2026-01-09	Warnings	Exact identifier application number: M020
Mineral Sunscreen SPF 30	ZINC OXIDE	Supergoop, LLC	4cf243b4-d794-401a-b209-18c7e550ef4f	2026-01-09	Warnings	Exact identifier application number: M020
Daily Dose Bioretinol Mineral SPF 40	ZINC OXIDE	Supergoop, LLC	eb5bbc70-dbdf-06a8-e053-2995a90a66c1	2026-01-09	Warnings	Exact identifier application number: M020
Unseen Sunscreen Body SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	ec1c30bd-76e1-9d00-e053-2a95a90a1759	2026-01-09	Warnings	Exact identifier application number: M020
Glow Screen SPF 40	AVOBENZONE, OCTISALATE, OCTOCYLENE	Supergoop, LLC	21569637-332a-461b-bf6c-33af6a83a155	2026-01-09	Warnings	Exact identifier application number: M020
Glowscreen SPF 40 - Dawn	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	f07145d5-b74d-7757-e053-2a95a90ac4c0	2026-01-09	Warnings	Exact identifier application number: M020
Glowscreen SPF 40 -Sunset	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	f7e493da-8fc6-191d-e053-6294a90aa483	2026-01-09	Warnings	Exact identifier application number: M020
Supergoop Glow Screen SPF 40 Shade 2 Golden Hour	BROAD SPECTRUM SUNSCREEN	Supergoop LLC	d2928dd7-a813-4929-e053-2a95a90aaeb4	2026-01-09	Warnings	Exact identifier application number: M020
Superscreen Hydrating Daily Cream SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	ff0e4e97-8f01-bd36-e053-6394a90a47ae	2026-01-09	Warnings	Exact identifier application number: M020
Lipshade SPF 30 Hey Yall	ZINC OXIDE	Supergoop, LLC	f93dfa13-ff18-ee38-e053-6394a90aea46	2026-01-09	Warnings	Exact identifier application number: M020
Triple Prep SPF 40	AVOBENZONE, OCTISALATE, OCTOCRYLENE, HOMOSALATE	Supergoop, LLC	004df4e5-dba9-6030-e063-6394a90a76d3	2026-01-09	Warnings	Exact identifier application number: M020
Unseen Sunscreen Lip Protector SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	12605fb4-0de6-94f3-e063-6294a90a3a6f	2026-01-09	Warnings	Exact identifier application number: M020
Unseen Sunscreen Stick SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	2735c5c7-a4ef-33c3-e063-6294a90abf97	2026-01-09	Warnings	Exact identifier application number: M020
PLAY Sunscreen SPF 50	HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE	Supergoop LLC	2860d42c-d644-8b5a-e063-6394a90aec10	2026-01-09	Warnings	Exact identifier application number: M020
PLAY Mineral SPF 30 with Green Algae	ZINC OXIDE	Supergoop LLC	29a1ff4b-3875-5275-e063-6394a90a53fd	2026-01-09	Warnings	Exact identifier application number: M020
Every. Single. Face. Watery SPF 50	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Supergoop, LLC	d086a9b8-19e5-f713-e053-2995a90aa976	2026-01-09	Warnings	Exact identifier application number: M020
3D Tinted Moisturizing BS SPF 30	ZINC OXIDE	Allure Labs	47fd415f-819e-bbb8-e063-6394a90a2c6a	2026-01-09	Warnings	Exact identifier application number: M020
ST MORIZ SUNCARE BODY SUNSCREEN SPF50	SUNCARE BODY SUNSCREEN SPF50	Aopline Biotechnology (Guangzhou) Co., Ltd.	4801cfd2-1fe2-d118-e063-6294a90a6c8b	2026-01-09	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE

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