Avon Anew Platinum Day Broad Spectrum SPF 25 Sunscreen

Product NDC: 10096-0550
11-digit product format: 100960550
Labeler code: 10096
Product ID: 10096-0550_e00ab2a9-3e6d-2fb6-e053-2a95a90a8819
Type: HUMAN OTC DRUG
Nonproprietary name: Avobenzone, Octinoxate, Octisalate, Oxybenzone
Dosage form: CREAM
Route: TOPICAL
Labeler: New Avon LLC
Application: part352
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2022-05-27
Marketing end: 0000-00-00
Substance: AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE
Active strength: 3 mg/g; mg/g; mg/g; mg/g
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	10096-0550		D	Discontinued by firm		2026-09-14
excluded package	package	10096-0550	10096-0550-1	D	Discontinued by firm		2026-09-14

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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product	10096-0550		I	Inactivated by FDA		excluded / ndc_excluded.zip	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	10096-0550	10096-0550-1	I	Inactivated by FDA		excluded / ndc_excluded.zip	`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
10096-0550-1	2024-03-25	C162847	48780-1	1030e365-5680-111a-e063-dadaa90a10e2	Avon Anew Platinum Day Cream SPF 25 50g
10096-0550-1	2024-01-30	C162847	48780-1	1030e365-5680-111a-e063-dadaa90a10e2	Avon Anew Platinum Day Cream SPF 25 50g

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10096-0550	AVON ANEW PLATINUM DAY BROAD SPECTRUM SPF 25 SUNSCREEN (AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE) CREAM [THE AVON COMPANY]	2	Legacy NDC	20240327_e00ad1b5-7162-6a56-e053-2995a90a2e6e.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
95OOS7VE0Y	OXYBENZONE	131-57-7	OXYBENZONE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
10096-0550-1	10096055001	50 g in 1 JAR (10096-0550-1)	50 g	2022-05-27	0000-00-00	No	No	Current