Reef Repair SPF 30

Product NDC: 73541-001
11-digit product format: 735410001
Labeler code: 73541
Product ID: 73541-001_cdb3fa8b-eb83-df4c-e053-2995a90a670f
Type: HUMAN OTC DRUG
Nonproprietary name: Zinc Oxide, 20%
Dosage form: CREAM
Route: TOPICAL
Labeler: Alive 2 Dive Company Limited
Application: part352
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2019-12-27
Marketing end: 0000-00-00
Substance: ZINC OXIDE
Active strength: 20 g/100mL
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	73541-001		I	Inactivated by FDA		2026-10-05
excluded package	package	73541-001	73541-001-01	I	Inactivated by FDA		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, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	73541-001-01	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	73541-001-01	`f5e01cc5f278…`	`a2eaf40c39c3…`

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
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73541-001-01	2025-07-29	C162847	48780-1	ba0f9c33-2129-a910-e053-dadaa90a0b85	Reef Repair Suncream SPF 30+
73541-001-01	2021-10-06	C162847	48780-1	ba0f9c33-2129-a910-e053-dadaa90a0b85	Reef Repair Suncream SPF 30+
73541-001-01	2021-01-29	C162847	48780-1	ba0f9c33-2129-a910-e053-dadaa90a0b85	Reef Repair Suncream SPF 30+

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73541-001-01	Reef Repair SPF 30Suncream	120 mL in 1 BOTTLE	CREAM	120		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73541-001	REEF REPAIR SPF 30 SUNCREAM (ZINC OXIDE, 20%) CREAM [ALIVE 2 DIVE COMPANY LIMITED]	4	Legacy NDC, 1 package rows	20240410_996fc76e-bd7e-305b-e053-2995a90ac103.zip

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
73541-001-01	73541000101	120 mL in 1 BOTTLE (73541-001-01)	120 ml	2019-12-27	0000-00-00	No	No	Current