Obagi Medical Physical Defense Broad Spectrum Mineral Sunscreen SPF 40 by SUZANOBAGIMD

Product NDC: 62032-607
Requested package NDC: 62032-607-35
11-digit product format: 620320607
Labeler code: 62032
Product ID: 62032-607_f814f248-217b-4ea2-ae6c-90e598319da7
Type: HUMAN OTC DRUG
Nonproprietary name: Titanium Dioxide and Zinc Oxide
Dosage form: CREAM
Route: TOPICAL
Labeler: Obagi Cosmeceuticals LLC
Application: part352
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2020-04-01
Marketing end: 0000-00-00
Substance: TITANIUM DIOXIDE; ZINC OXIDE
Active strength: 45 mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2022-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	62032-607	62032-607-35	D	Discontinued by firm		2026-10-05

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 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2025-03-10 12:48 UTC · source 2025-03-10	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	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
62032-607-35	2025-03-14	C162847	48780-1	2cef2736-a985-d83d-e063-dadaa90ab31f	Obagi ® Medical Physical Defense Broad Spectrum Mineral Sunscreen SPF 40 by SUZANOBAGIMD
62032-607-35	2025-01-30	C162847	48780-1	2cef2736-a985-d83d-e063-dadaa90ab31f	Obagi ® Medical Physical Defense Broad Spectrum Mineral Sunscreen SPF 40 by SUZANOBAGIMD

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62032-607	OBAGI MEDICAL PHYSICAL DEFENSE BROAD SPECTRUM MINERAL SUNSCREEN SPF 40 BY SUZANOBAGIMD (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [OBAGI COSMECEUTICALS LLC]	3	Legacy NDC	20250316_ac41a94d-6a07-4b6f-a962-0fa2c5a4b99f.zip

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
62032-607-35	62032060735	1 TUBE in 1 CARTON (62032-607-35) > 96.3 g in 1 TUBE	1 tube	2020-04-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Titanium Dioxide and Zinc Oxide	Obagi Cosmeceuticals LLC \| G.S.COSMECEUTICAL USA, INC.	2025-01-01	HUMAN OTC DRUG LABEL	3