NDC 10096-0266

Anew Ultimate 7S Day

Homosalate, Octinoxate, Oxybenzone, Avobenzone

Anew Ultimate 7S Day is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Avon Products, Inc.. The primary component is Homosalate; Octinoxate; Oxybenzone; Avobenzone.

• Product ID: 10096-0266_c9edc5e4-b478-4485-9f95-4c25d44c9720
• NDC: 10096-0266
• Product Type: Human Otc Drug
• Proprietary Name: Anew Ultimate 7S Day
• Generic Name: Homosalate, Octinoxate, Oxybenzone, Avobenzone
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2011-12-20
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: Avon Products, Inc.
• Substance Name: HOMOSALATE; OCTINOXATE; OXYBENZONE; AVOBENZONE
• Active Ingredient Strength: 4 g/50g; g/50g; g/50g; g/50g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 10096-0266-2

1 JAR in 1 CARTON (10096-0266-2) > 50 g in 1 JAR (10096-0266-1)

• Marketing Start Date: 2011-12-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10096-0266-3 [10096026603]

Anew Ultimate 7S Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-20

NDC 10096-0266-4 [10096026604]

Anew Ultimate 7S Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-20
• Inactivation Date: 2019-11-13

NDC 10096-0266-1 [10096026601]

Anew Ultimate 7S Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-20

NDC 10096-0266-2 [10096026602]

Anew Ultimate 7S Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-20
• Inactivation Date: 2019-11-13

NDC 10096-0266-5 [10096026605]

Anew Ultimate 7S Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-12-20
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
HOMOSALATE	4 g/50g

OpenFDA Data

• SPL SET ID: fac8fdd9-fb1c-46c6-82ad-bef24ed35ddd
• Manufacturer:
  • Avon Products, Inc.
• UNII:
  • G63QQF2NOX
  • 95OOS7VE0Y
  • V06SV4M95S
  • 4Y5P7MUD51

NDC Crossover Matching brand name "Anew Ultimate 7S Day" or generic name "Homosalate, Octinoxate, Oxybenzone, Avobenzone"

NDC	Brand Name	Generic Name
10096-0266	Anew	HOMOSALATE, OCTINOXATE, OXYBENZONE, AVOBENZONE
10096-0311	Anew Reversalist	Homosalate, Octinoxate, Oxybenzone, Avobenzone
10096-0312	Anew Reversalist	Homosalate, Octinoxate, Oxybenzone, Avobenzone
71110-0010	Anew Reversalist	Homosalate, Octinoxate, Oxybenzone, Avobenzone
10096-0323	Anew Ultimate	Homosalate, Octinoxate, Oxybenzone, Avobenzone
71110-0013	Anew Ultimate	Homosalate, Octinoxate, Oxybenzone, Avobenzone
10096-0322	Anew Vitale	Homosalate, Octinoxate, Oxybenzone, Avobenzone
71110-0017	Anew Vitale	Homosalate, Octinoxate, Oxybenzone, Avobenzone
10096-0318	Avon Elements	Homosalate, Octinoxate, Oxybenzone, Avobenzone
64141-916	BOBBI BROWN EXTRA	HOMOSALATE, OCTINOXATE, OXYBENZONE, AVOBENZONE