WATERMELON GLOW NIACINAMIDE SUNSCREEN

Product NDC: 72156-002
11-digit product format: 721560002
Labeler code: 72156
Product ID: 72156-002_9d5276a8-7bb9-4ef4-ae1e-1990d03f2aff
Type: HUMAN OTC DRUG
Nonproprietary name: Homosalate, Octisalate, Octocrylene, and Zinc Oxide
Dosage form: LOTION
Route: TOPICAL
Labeler: Aramara Beauty
Application: part352
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2022-02-22
Marketing end: 0000-00-00
Substance: HOMOSALATE; OCTISALATE; OCTOCRYLENE; ZINC OXIDE
Active strength: 85 mg/mL; mg/mL; mg/mL; mg/mL
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	72156-002		I	Inactivated by FDA		2026-10-05
excluded package	package	72156-002	72156-002-01	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 · 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	72156-002-01	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	72156-002-01	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	72156-002-01	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	72156-002-01	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	72156-002-01	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	72156-002-01	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	72156-002-01	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	72156-002-01	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	72156-002-01	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
72156-002-01	2025-01-30	C162847	48780-1	0191ceaa-6e35-198a-e063-dbdaa90aec3e	WATERMELON GLOW NIACINAMIDE SUNSCREEN™
72156-002-01	2023-12-21	C162847	48780-1	0191ceaa-6e35-198a-e063-dbdaa90aec3e	WATERMELON GLOW NIACINAMIDE SUNSCREEN™
72156-002-01	2023-07-28	C162847	48780-1	0191ceaa-6e35-198a-e063-dbdaa90aec3e	WATERMELON GLOW NIACINAMIDE SUNSCREEN™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72156-002-00	WATERMELON GLOW NIACINAMIDE SUNSCREEN	50 mL in 1 TUBE	LOTION	50		3
72156-002-01	WATERMELON GLOW NIACINAMIDE SUNSCREEN	1 in 1 CARTON	LOTION	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72156-002	WATERMELON GLOW NIACINAMIDE SUNSCREEN (HOMOSALATE, OCTISALATE, OCTOCRYLENE, AND ZINC OXIDE) LOTION [ARAMARA BEAUTY]	3	Legacy NDC, 2 package rows	20231222_7b5c10c4-5362-4314-ab6a-1c4fcaed8f42.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
5A68WGF6WM	OCTOCRYLENE	6197-30-4	OCTOCRYLENE
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
72156-002-00	72156000200	50 mL in 1 TUBE	50 ml					Historical
72156-002-01	72156000201	1 TUBE in 1 CARTON (72156-002-01) > 50 mL in 1 TUBE (72156-002-00)	1 tube	2022-02-22	0000-00-00	No	No	Current