Cream

Product NDC: 61354-084
11-digit product format: 613540084
Labeler code: 61354
Product ID: 61354-084_e7763ac1-d05c-7f8f-e053-2995a90a6c15
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide, Titanium Dioxide
Dosage form: CREAM
Route: TOPICAL
Labeler: Oxygen Development LLC
Application: M020
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2022-08-30
Marketing end: 0000-00-00
Substance: TITANIUM DIOXIDE; ZINC OXIDE
Active strength: 5 mg/100mg; mg/100mg
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	61354-084		I	Inactivated by FDA		2026-10-30
excluded package	package	61354-084	61354-084-01	I	Inactivated by FDA		2026-10-30

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 · 18 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	61354-084-01	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	61354-084-01	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	61354-084-01	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	61354-084-01	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	61354-084-01	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	61354-084-01	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	61354-084-01	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	61354-084-01	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	61354-084-01	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
61354-084-01	2025-01-30	C162847	48780-1	2cef2736-62bf-d83d-e063-dadaa90ab31f	TARTE high-performance naturals BB tinted treatment primer Broad Spectrum SPF 30 Sunscreen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
61354-084-01	Cream	100 mg in 1 TUBE	CREAM	100		1
61354-084-01	Cream	1 in 1 CARTON	CREAM	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
61354-084	CREAM (ZINC OXIDE, TITANIUM DIOXIDE) CREAM [OXYGEN DEVELOPMENT LLC]	1	Legacy NDC, 2 package rows	20220831_e7760899-8b4a-9a2a-e053-2995a90a2fd5.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 289 of 353 · 7,041 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Walgreens Daytime Facial Moisturizer with Broad Spectrum SPF 30 Sunscreen	HOMOSALATE, OCTOCRYLENE, ZINC OXIDE	WALGREEN COMPANY	f9c81d88-8e28-fa53-e053-6394a90ac5c4	2024-10-11	Warnings	Exact identifier application number: M020
WALGREENS 100 SHEER BROAD SPECTRUM SPF 100	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	fa18067a-310b-bdc3-e053-6394a90aee79	2024-10-11	Warnings	Exact identifier application number: M020
Walgreens 50 Mineral Zinc Oxide Sunscreen	ZINC OXIDE	WALGREEN COMPANY	24223fbf-8ce9-ec5e-e063-6294a90a29da	2024-10-10	Warnings	Exact identifier application number: M020
Walgreens 50 Mineral Zinc Oxide Sunscreen	ZINC OXIDE	WALGREEN COMPANY	2422b327-ea83-f4c3-e063-6394a90a5c6e	2024-10-10	Warnings	Exact identifier application number: M020
Walgreens 50 Watermelon Scented Continuous Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	24256e54-ae34-91b2-e063-6394a90a33c0	2024-10-10	Warnings	Exact identifier application number: M020
Walgreens 50 Premium Face Moisturizing Sunscreen	AVOBENZONE. HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	24265a48-fd07-c78a-e063-6394a90ab67e	2024-10-10	Warnings	Exact identifier application number: M020
Walgreens Broad Spectrum SPF 50 Body Oil Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	2410df0a-db52-0769-e063-6394a90a52f3	2024-10-09	Warnings	Exact identifier application number: M020
Walgreens Broad Spectrum SPF 40 Radiant Facial Sunscreen	AVOBENZONE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	24114416-33b9-c6ba-e063-6394a90a6f3b	2024-10-09	Warnings	Exact identifier application number: M020
Walgreens 40 Invisible Facial Sunscreen Broad Spectrum SPF 40	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	WALGREEN COMPANY	0c40a46b-b9f9-8e14-e063-6394a90a9573	2024-10-09	Warnings	Exact identifier application number: M020
AMOREPACIFIC COLOR CONTROL CUSHION COMPACT NO.102	ZINC OXIDE, OCTINOXATE, AND TITANIUM DIOXIDE	AMOREPACIFIC CORPORATION	531f60c9-c89a-46bc-8460-d01b2e838e6f	2024-10-08	Warnings	Exact identifier application number: M020
AMOREPACIFIC COLOR CONTROL CUSHION COMPACT NO.104	OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE	AMOREPACIFIC CORPORATION	60964d9f-d96c-4397-b273-6b63d1886722	2024-10-08	Warnings	Exact identifier application number: M020
IOPE AIR CUSHION Cover 21 Vanilla	ZINC OXIDE, OCTINOXATE, AND TITANIUM DIOXIDE	AMOREPACIFIC CORPORATION	29d6cc8d-1469-479d-a15a-e78d4e22d4a2	2024-10-08	Warnings	Exact identifier application number: M020
IOPE UV DEFENSE SUN PROTECTOR	HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE	AMOREPACIFIC CORPORATION	0f2a87f7-2185-16a5-e063-6294a90a92a3	2024-10-08	Warnings	Exact identifier application number: M020
Tropical Topical Matte SPF30	ZINC OXIDE	Allure Labs	039fba4b-720a-9199-e063-6394a90adbfb	2024-10-08	Warnings	Exact identifier application number: M020
LANEIGE HYDRO UV DEFENSE EX BROAD SPECTRUM SPF 50	OCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONE	AMOREPACIFIC CORPORATION	0e746836-ed84-7b33-e063-6294a90aeff3	2024-10-08	Warnings	Exact identifier application number: M020
DermacinRx Skin Moisturizing Ultra SPF 50 Sunscreen	AVOBENZONE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE	PureTek Corporation	86eb06cc-d63f-4500-a52e-14ef99a56532	2024-10-02	Warnings	Exact identifier application number: M020
TiZO2	TITANIUM DIOXIDE, ZINC OXIDE	Fallien Cosmeceuticals, LTD	43bec652-3f2c-4671-8a0c-c4c4a4bfcc7a	2024-10-01	Warnings	Exact identifier application number: M020
PROCEUTICALS PRIVATE LABEL by TiZO eye repair non-tinted mineral sunscreen	ZINC OXIDE	Fallien Cosmeceuticals, LTD	231af290-99ee-e94d-e063-6394a90a0bef	2024-09-27	Warnings	Exact identifier application number: M020
Target Up and Up SPF 70 Sport Sunscreen	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	TARGET CORPORATION	23085ab9-5abb-a572-e063-6394a90ae34a	2024-09-26	Warnings	Exact identifier application number: M020
Target Up and Up Morning Facial Moisturizing with SPF 30 Sunscreen and Ceramides	HOMOSALATE, OCTOCRYLENE, ZINC OXIDE	TARGET CORPORATION	23598ad1-12a3-fe65-e063-6394a90a4f6f	2024-09-26	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
15FIX9V2JP	TITANIUM DIOXIDE	13463-67-7	TITANIUM DIOXIDE
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
61354-084-01	61354008401	1 TUBE in 1 CARTON (61354-084-01) > 100 mg in 1 TUBE	1 tube	2022-08-30	0000-00-00	No	No	Current