Cream

Product NDC: 78518-007
11-digit product format: 785180007
Labeler code: 78518
Product ID: 78518-007_46e05ccb-82a8-f692-e063-6294a90a079a
Type: HUMAN OTC DRUG
Nonproprietary name: ZINC OXIDE
Dosage form: CREAM
Route: TOPICAL
Labeler: MONAT GLOBAL CORP
Application: M020
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-09-12
Substance: ZINC OXIDE
Active strength: 18.8 mg/100mg
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 · 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	78518-007-01	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	78518-007-01	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	78518-007-01	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	78518-007-01	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	78518-007-01	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	78518-007-01	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	78518-007-01	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	78518-007-01	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	78518-007-01	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: Cream
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ZINC OXIDE	18.8 mg/100mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
SOI2LOH54Z	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
e9231470-9292-0e70-e053-2a95a90a767a	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d1c9d1af-bddd-448d-86f7-69052b7d5b47	Product name	1	20220627
124351b2-6dbf-42d0-9ea7-f0e299215f9a	Product name	1	20210115

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2025-12-26	BB Cream SPF 40 Broad-Spectrum Moisturizer (Porcelain)
2025-01-30	BB Cream SPF 40 Broad-Spectrum Moisturizer (Porcelain)
2023-08-11	BB Cream SPF 40 Broad-Spectrum Moisturizer (Porcelain)
2023-07-28	BB Cream SPF 40 Broad-Spectrum Moisturizer (Porcelain)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78518-007-01	Cream	1 in 1 CARTON	CREAM	1		3
78518-007-01	Cream	35 mg in 1 TUBE	CREAM	35		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78518-007	CREAM (ZINC OXIDE) CREAM [MONAT GLOBAL CORP]	2	Current NDC, Legacy NDC, 2 package rows	20230812_e9231470-9292-0e70-e053-2a95a90a767a.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 98 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eucerin Daily Hydration	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Beiersdorf Inc	798cbf7f-b93d-49c8-b1c1-216486e57ea5	2025-12-31	Warnings	Exact identifier application number: M020
Eucerin Face immersive Hydration	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Beiersdorf Inc	fe0b3717-f472-3a61-e053-6394a90a44fb	2025-12-31	Warnings	Exact identifier application number: M020
NIVEA MEN Age Defense Face Moisturizer	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	Beiersdorf Inc	27cbec3e-e811-6498-e063-6394a90ada49	2025-12-31	Warnings	Exact identifier application number: M020
Nivea Men Maximum Hydration Face	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Beiersdorf Inc	f1276b11-6683-e982-e053-2a95a90a7803	2025-12-31	Warnings	Exact identifier application number: M020
Nivea Men Sensitive Protective	AVOBENZONE, OCTISALATE, OCTOCRYLENE	Beiersdorf Inc	f6cff3d1-cca5-4b3e-a481-0c4def90684c	2025-12-31	Warnings	Exact identifier application number: M020
Nivea Smoothness Lip Care	AVOBENZONE,OCTOCRYLENE	Beiersdorf Inc	c28e327d-ad39-9bd6-e053-2a95a90a04eb	2025-12-31	Warnings	Exact identifier application number: M020
BOTANICAL SOOTHING SPF-30	OCTINOXATE, OCTISALATE, ZINC OXIDE	CONTROL CORRECTIVE SKINCARE INC	00a923fe-e6da-420e-a705-4773ecc2176b	2025-12-31	Warnings	Exact identifier application number: M020
AROMA MATTE DAY SUNSCREEN SPF-30	OCTINOXATE, OCTISALATE, ZINC OXIDE	CONTROL CORRECTIVE SKINCARE INC	f822f3ec-3c57-100a-e053-6294a90ab0ec	2025-12-31	Warnings	Exact identifier application number: M020
CONTROL CORRECTIVE TINTED MOISTURIZER SPF-30 SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	CONTROL CORRECTIVE SKINCARE INC	8ac09149-f7e7-40a8-b306-98964d0cd6e3	2025-12-31	Warnings	Exact identifier application number: M020
CONTROL CORRECTIVE SUNSCREEN SPF-30	OCTINOXATE, OCTISALATE, ZINC OXIDE	CONTROL CORRECTIVE SKINCARE INC	e389b2bc-bb1c-443a-9bf6-c6d96380f378	2025-12-31	Warnings	Exact identifier application number: M020
CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING SPF-30 SUNSCREEN	OCTINOXATE, OCTISALATE, ZINC OXIDE	CONTROL CORRECTIVE SKINCARE INC	61b6dab9-3378-4206-bf1f-6f385a9c882c	2025-12-31	Warnings	Exact identifier application number: M020
Blue Lizard Sensitive SPF 50 Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	Crown Laboratories	32d78048-d281-1d80-e063-6394a90aec19	2025-12-31	Warnings	Exact identifier application number: M020
DAYWEAR ANTI OXIDANT 72H-HYDRATION SORBET CREME BROAD SPECTRUM SPF 15	AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE	ESTEE LAUDER INC	df535004-c94c-4a28-ad20-78bd1741e39f	2025-12-31	Warnings	Exact identifier application number: M020
FUTURIST SKIN TINT SERUM	OCTINOXATE,OCTISALATE,ZINC OXIDE	ESTEE LAUDER INC	ea21e5a5-69d6-2de4-e053-2995a90a93b4	2025-12-31	Warnings	Exact identifier application number: M020
Dr.Jart Cicapair Tiger Grass Color Correcting Treatment	ZINC OXIDE, TITANIUM DIOXIDE	Have & Be Co., Ltd.	40f96baf-0359-4d68-801f-68562c909446	2025-12-31	Warnings	Exact identifier application number: M020
Dr.Jart Premium Beauty Balm Fair-Light	ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	Have & Be Co., Ltd.	b38b1b64-b433-4e11-9cf6-2108a552d139	2025-12-31	Warnings	Exact identifier application number: M020
Dr.Jart Premium Beauty Balm Light Medium-Medium	ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	Have & Be Co., Ltd.	45b1c2c6-a45b-4a45-bec9-e5341079c0a1	2025-12-31	Warnings	Exact identifier application number: M020
Dr.Jart Premium Beauty Balm Medium-Tan	ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	Have & Be Co., Ltd.	28a2ba45-1eff-488c-aae4-362b9f78b8df	2025-12-31	Warnings	Exact identifier application number: M020
Dr.Jart Premium Beauty Balm Deep Tan-Deep	ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	Have & Be Co., Ltd.	3c346960-b76b-4241-a188-8ee694853078	2025-12-31	Warnings	Exact identifier application number: M020
DR.JART CICAPAIR TIGER GRASS CAMO DROPS	ZINC OXIDE, TITANIUM DIOXIDE	Have & Be Co., Ltd.	f06348f5-4ebc-325b-e053-2a95a90ada52	2025-12-31	Warnings	Exact identifier application number: M020

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
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
78518-007-01	78518000701	1 TUBE in 1 CARTON (78518-007-01) / 35 mg in 1 TUBE	1 tube	2022-09-12	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
BB Cream SPF 40 Broad-Spectrum Moisturizer (Porcelain)	MONAT GLOBAL CORP \| OXYGEN DEVELOPMENT, LLC	2025-12-26	HUMAN OTC DRUG LABEL	3