Hydraboost Oil-Free Sunscreen SPF 40

Product NDC: 72203-015
Requested package NDC: 72203-015-01
11-digit product format: 722030015
Labeler code: 72203
Product ID: 72203-015_cce77037-95be-4ca4-81e6-0808d5b507d0
Type: HUMAN OTC DRUG
Nonproprietary name: HOMOSALATE, OCTISALATE, and AVOBENZONE
Dosage form: LOTION
Route: TOPICAL
Labeler: Bluemercury
Application: part352
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2021-04-01
Marketing end: 0000-00-00
Substance: HOMOSALATE; OCTISALATE; AVOBENZONE
Active strength: 145 mg/mL; mg/mL; mg/mL
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	72203-015	72203-015-01	D	Discontinued by firm		2026-10-16

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 · 8 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`

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
72203-015-01	2025-01-29	C162847	48780-1	1030e365-08d6-111a-e063-dadaa90a10e2	Hydraboost Oil-Free Sunscreen SPF 40
72203-015-01	2024-01-30	C162847	48780-1	1030e365-08d6-111a-e063-dadaa90a10e2	Hydraboost Oil-Free Sunscreen SPF 40

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72203-015	HYDRABOOST OIL-FREE SUNSCREEN SPF 40 (HOMOSALATE, OCTISALATE, AND AVOBENZONE) LOTION [BLUEMERCURY]	3	Legacy NDC	20250130_b14f0305-cd4f-4de8-926f-b898f143c494.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72203-015-01	72203001501	1 BOTTLE in 1 CARTON (72203-015-01) > 50 mL in 1 BOTTLE	1 bottle	2021-04-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Hydraboost Oil-Free Sunscreen SPF 40	Bluemercury \| Biogenesis, Inc.	2025-12-09	HUMAN OTC DRUG LABEL	4