COSRX

Product NDC: 70319-220
11-digit product format: 703190220
Labeler code: 70319
Product ID: 70319-220_4415daaf-9353-7695-e063-6394a90ad88c
Type: HUMAN OTC DRUG
Nonproprietary name: Vitamin E Vitalizing Sunscreen
Dosage form: LOTION
Route: TOPICAL
Labeler: COSRX inc.
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2025-12-01
Substance: AVOBENZONE; OCTOCRYLENE; HOMOSALATE; OCTISALATE
Active strength: 1.25; 2.25; 4.5; 4.5 mg/50mL; mg/50mL; mg/50mL; mg/50mL
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	70319-220-01	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	70319-220-01	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	70319-220-01	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	70319-220-01	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	70319-220-01	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	70319-220-01	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	70319-220-01	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: COSRX
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
AVOBENZONE	1.25 mg/50mL
OCTOCRYLENE	2.25 mg/50mL
HOMOSALATE	4.5 mg/50mL
OCTISALATE	4.5 mg/50mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 4 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
G63QQF2NOX	Internal UNII lookup
5A68WGF6WM	Internal UNII lookup
V06SV4M95S	Internal UNII lookup
4X49Y0596W	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
daf0291e-770c-eaf2-e053-2a95a90a0b67	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
cb89b86a-369e-4204-8910-ae797c503af3	Product name	1	20230706
d4880ace-a516-8c47-8dfd-73a4ba5887d7	Product name	2	20180830
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
70319-220-01	2025-01-30	C162847	48780-1	2cef2736-9f9c-d83d-e063-dadaa90ab31f	daf0291e-770c-eaf2-e053-2a95a90a0b67

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70319-220-01	COSRX	1 in 1 CARTON	LOTION	1		6
70319-220-01	COSRX	50 mL in 1 TUBE	LOTION	50		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70319-220	COSRX (VITAMIN E VITALIZING SUNSCREEN) LOTION [COSRX INC.]	5	Current NDC, Legacy NDC, 2 package rows	20250523_daf0291e-770c-eaf2-e053-2a95a90a0b67.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 38 of 357 · 7,139 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
RE SCREEN BROAD SPECTRUM SPF 30 SUNSCREEN	ZINC OXIDE	Zouck LLC	507560fe-c7ad-329a-e063-6394a90a039a	2026-04-27	Warnings	Exact identifier application number: M020
SoloVegan	HOMOSALATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE	YES SALES INC.	435748e6-c39a-efee-e063-6294a90ad0e5	2026-04-27	Warnings	Exact identifier application number: M020
SCREEN SCREEN BROAD SPECTRUM SPF 30 SUNSCREEN	ZINC OXIDE	Zouck LLC	50764f40-7881-81a3-e063-6294a90ad1cf	2026-04-27	Warnings	Exact identifier application number: M020
Obagi Skintrinsiq Antioxidant Protocol	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND OXYBENZONE	Obagi Cosmeceuticals LLC	495bc176-b292-448f-a5a6-00de2e475e54	2026-04-27	Warnings	Exact identifier application number: M020
TULA RADIANT SKIN BRIGHTENING SERUM SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30	BRIGHTENING SKIN TINT	PML NYC, LLC	f45bd7bd-a802-33e4-e053-2a95a90a61a7	2026-04-23	Warnings	Exact identifier application number: M020
TRACELESS MINERAL BROAD SPECTRUM SPF SUNSCREEN AND PRIMER	TRACELESS MINERAL BROAD SPECTRUM SPF SUNSCREEN AND PRIMER	PML NYC, LLC	1c2e9b0d-ba0e-1767-e063-6394a90a756c	2026-04-23	Warnings	Exact identifier application number: M020
Skincare LdeL Retinol Day Broad Spectrum SPF 20	AVOBENZONE, HOMOSALATE, OXYBENZONE, AND OCTINOXATE	Beauty Solutions, Ltd.	76e2ed34-c643-402b-9c9d-04eac789d3c2	2026-04-22	Warnings	Exact identifier application number: M020
Johnsons Baby Mineral Sunscreen SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Kenvue Brands LLC	4fe04c4b-2751-0561-e063-6394a90af768	2026-04-22	Warnings	Exact identifier application number: M020
Johnsons Baby Mineral Sunscreen Stick SPF 50	ZINC OXIDE	Kenvue Brands LLC	4fe1d3c6-7748-d966-e063-6394a90a97ff	2026-04-22	Warnings	Exact identifier application number: M020
OVERLAPS ECTOIN MOIST SUN	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Overlaps Corp.	4c3ed60b-e515-8ff0-e063-6294a90a86df	2026-04-22	Warnings	Exact identifier application number: M020
Lazy Face SPF 30 Facescreen	TITANIUM DIOXIDE, ZINC OXIDE	Sunny Day Creations	500ee303-7302-68d5-e063-6394a90ac6d4	2026-04-22	Warnings	Exact identifier application number: M020
Lazy Face SPF 30 Facestick	ZINC OXIDE	Sunny Day Creations	50101b55-793e-dbe4-e063-6394a90a6199	2026-04-22	Warnings	Exact identifier application number: M020
Broad Spectrum Sunscreen SPF 30	OCTOCRYLENE 10% HOMOSALATE 10% OCTISALATE 5 % AVOBENZONE 3%	S&C Hampton Sun LLC	e6103de6-1d80-46fd-b9d4-893f60941def	2026-04-22	Warnings	Exact identifier application number: M020
PhotoAge Guard	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE	MACROMOTION, INC.	50164bd8-469d-9ec1-e063-6294a90a543d	2026-04-22	Warnings	Exact identifier application number: M020
THANK YOU FARMER Sun Project Silky Calming Sun Stick	AVOBENZONE, OCTISALATE, HOMOSALATE, OCTOCRYLENE	THANK YOU FARMER CO., LTD	49947114-5137-dc45-e063-6394a90ad9d0	2026-04-22	Warnings	Exact identifier application number: M020
Sky and Sol Intense Healing Lip Jelly	NON-NANO ZINC OXIDE	Delta Ecommerce LLC	2ddaa215-7433-c8fa-e063-6394a90a4316	2026-04-22	Warnings	Exact identifier application number: M020
Broad Spectrum SPF45	ZINC OXIDE, OCTINOXATE	Drmtlgy, LLC	0445ee5f-45a8-4fd5-ae4d-62f66e6f0be8	2026-04-21	Warnings	Exact identifier application number: M020
BLDG Active Skin Repair Face and Body Performance Sunscreen	ZINC OXIDE	Innovacyn, Inc.	70cb98cf-739b-4d46-b45a-535ff0a4531c	2026-04-21	Warnings	Exact identifier application number: M020
Freaks of Nature Mineral Sunscreen	ZINC OXIDE MINERAL SUNSCREEN	Empack Spraytech Inc.	4ffdb1c6-b2c6-628f-e063-6394a90a2769	2026-04-21	Warnings	Exact identifier application number: M020
THANK YOU FARMER Sun Project Water Sun Cream	AVOBENZONE, ETHYLHEXYL SALICYLATE, HOMOSALATE, OCTOCRYLENE	THANK YOU FARMER CO., LTD	5004126b-0a9c-21fb-e063-6294a90a5237	2026-04-21	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
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70319-220-01	70319022001	1 TUBE in 1 CARTON (70319-220-01) / 50 mL in 1 TUBE	1 tube	2025-12-01	0000-00-00	No	No	Current