Avon Ultimate Day Multi-Performance SPF 25

Product NDC: 10096-0450
Requested package NDC: 10096-0450-1
11-digit product format: 100960450
Labeler code: 10096
Product ID: 10096-0450_e009cc4d-838c-4100-e053-2995a90a75a8
Type: HUMAN OTC DRUG
Nonproprietary name: Avobenzone, Homosalate, Octinoxate, 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; HOMOSALATE; OCTINOXATE; OXYBENZONE
Active strength: 3 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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	10096-0450	10096-0450-1	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 · 1 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 package	package	10096-0450	10096-0450-1	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
10096-0450-1	2024-03-25	C162847	48780-1	1030e365-28fd-111a-e063-dadaa90a10e2	Avon Anew Ultimate Multi-Performance Day Cream SPF 25 50g
10096-0450-1	2024-01-30	C162847	48780-1	1030e365-28fd-111a-e063-dadaa90a10e2	Avon Anew Ultimate Multi-Performance Day Cream SPF 25 50g

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10096-0450	AVON ULTIMATE DAY MULTI-PERFORMANCE SPF 25 (AVOBENZONE, HOMOSALATE, OCTINOXATE, OXYBENZONE) CREAM [THE AVON COMPANY]	2	Legacy NDC	20240327_e009cc3e-2f8b-b6cc-e053-2995a90a9562.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
G63QQF2NOX	AVOBENZONE	70356-09-1	AVOBENZONE
V06SV4M95S	HOMOSALATE	118-56-9	HOMOSALATE
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE
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
10096-0450-1	10096045001	50 mL in 1 JAR (10096-0450-1)	50 ml	2022-05-27	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Avon Anew Ultimate Multi-Performance Day Cream SPF 25 50g	The Avon Company	2024-01-01	HUMAN OTC DRUG LABEL	2