ANEW

Product NDC: 10096-0224
Requested package NDC: 10096-0224-7
11-digit product format: 100960224
Labeler code: 10096
Product ID: 10096-0224_8b85ed39-ffef-485e-e053-2995a90a9dd0
Type: HUMAN OTC DRUG
Nonproprietary name: OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
Dosage form: CREAM
Route: TOPICAL
Labeler: New Avon LLC
Application: part352
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2010-09-07
Marketing end: 0000-00-00
Substance: OCTINOXATE; OCTISALATE; OXYBENZONE; AVOBENZONE
Active strength: 75 mg/g; mg/g; mg/g; mg/g
NDC exclude flag: No
Listing certified through: 2020-12-31
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	10096-0224	10096-0224-7	I	Inactivated by FDA		2026-10-12

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, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
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…`
2022-08-30 03:57 UTC · source 2022-08-29	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
10096-0224-2	Anew Platinum Day Cream
10096-0224-4	Anew Platinum Day Cream
10096-0224-6	Anew Platinum Day Cream
10096-0224-7	Anew Platinum Day Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
10096-0224-1	ANEWPlatinum Day	50 g in 1 JAR	CREAM	50	5
10096-0224-2	ANEWPlatinum Day	1 in 1 CARTON	CREAM	1	5
10096-0224-3	ANEWPlatinum Day	15 g in 1 JAR	CREAM	15	5
10096-0224-4	ANEWPlatinum Day	1 in 1 CARTON	CREAM	1	5
10096-0224-5	ANEWPlatinum Day	7 g in 1 JAR	CREAM	7	5
10096-0224-6	ANEWPlatinum Day	1 in 1 CARTON	CREAM	1	5
10096-0224-7	ANEWPlatinum Day	1.1 g in 1 PACKET	CREAM	1.1	5

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
AVOBENZONE	ACTIVE INGREDIENT	G63QQF2NOX	ANEW PLATINUM DAY (OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [AVON PRODUCTS, INC.]	2
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	ANEW PLATINUM DAY (OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [AVON PRODUCTS, INC.]	2
OCTISALATE	ACTIVE INGREDIENT	4X49Y0596W	ANEW PLATINUM DAY (OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [AVON PRODUCTS, INC.]	2
OXYBENZONE	ACTIVE INGREDIENT	95OOS7VE0Y	ANEW PLATINUM DAY (OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [AVON PRODUCTS, INC.]	2
AVOBENZONE	ACTIVE MOIETY	G63QQF2NOX	ANEW PLATINUM DAY (OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [AVON PRODUCTS, INC.]	2
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	ANEW PLATINUM DAY (OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [AVON PRODUCTS, INC.]	2
OCTISALATE	ACTIVE MOIETY	4X49Y0596W	ANEW PLATINUM DAY (OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [AVON PRODUCTS, INC.]	2
OXYBENZONE	ACTIVE MOIETY	95OOS7VE0Y	ANEW PLATINUM DAY (OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [AVON PRODUCTS, INC.]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10096-0224	ANEW PLATINUM DAY (OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE) CREAM [NEW AVON LLC]	5	Legacy NDC, 7 package rows	20190617_9fb64ca8-b25e-4667-af12-6d7bbb6c93cd.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE
4X49Y0596W	OCTISALATE	118-60-5	OCTISALATE
95OOS7VE0Y	OXYBENZONE	131-57-7	OXYBENZONE
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
10096-0224-7	10096022407	1.1 g in 1 PACKET (10096-0224-7)	1.1 g	2010-09-07	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Anew Platinum Day Cream	New Avon LLC \| Fareva Morton Grove, Inc.	2019-01-01	HUMAN OTC DRUG LABEL	5