NDC 10096-0224

ANEW Platinum Day

Octinoxate, Octisalate, Oxybenzone, Avobenzone

ANEW Platinum Day is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by New Avon Llc. The primary component is Octinoxate; Octisalate; Oxybenzone; Avobenzone.

• Product ID: 10096-0224_8b85ed39-ffef-485e-e053-2995a90a9dd0
• NDC: 10096-0224
• Product Type: Human Otc Drug
• Proprietary Name: ANEW Platinum Day
• Generic Name: Octinoxate, Octisalate, Oxybenzone, Avobenzone
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-09-07
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: New Avon LLC
• Substance Name: OCTINOXATE; OCTISALATE; OXYBENZONE; AVOBENZONE
• Active Ingredient Strength: 75 mg/g; mg/g; mg/g; mg/g
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 10096-0224-2

1 JAR in 1 CARTON (10096-0224-2) > 50 g in 1 JAR (10096-0224-1)

• Marketing Start Date: 2019-09-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 10096-0224-3 [10096022403]

ANEW Platinum Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-02-14

NDC 10096-0224-6 [10096022406]

ANEW Platinum Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-09-07

NDC 10096-0224-7 [10096022407]

ANEW Platinum Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-09-07

NDC 10096-0224-1 [10096022401]

ANEW Platinum Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-09-07

NDC 10096-0224-5 [10096022405]

ANEW Platinum Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-02-14

NDC 10096-0224-2 [10096022402]

ANEW Platinum Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-09-07

NDC 10096-0224-4 [10096022404]

ANEW Platinum Day CREAM

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-09-07

Drug Details

Active Ingredients

Ingredient	Strength
OCTINOXATE	75 mg/g

OpenFDA Data

• SPL SET ID: 9fb64ca8-b25e-4667-af12-6d7bbb6c93cd
• Manufacturer:
  • New Avon LLC
• UNII:
  • G63QQF2NOX
  • 95OOS7VE0Y
  • 4X49Y0596W
  • 4Y5P7MUD51

NDC Crossover Matching brand name "ANEW Platinum Day" or generic name "Octinoxate, Octisalate, Oxybenzone, Avobenzone"

NDC	Brand Name	Generic Name
82084-0011	AGELESS SOLAR DEFENSE (SPF 30)	OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
10096-0224	ANEW	OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
71110-0009	ANEW	OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
10096-0305	Anew Rejuvenate	OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
10096-0181	Anew Reversalist	OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
10096-0319	Anew Vitale	Octinoxate, Octisalate, Oxybenzone, Avobenzone
71110-0008	Anew Vitale	Octinoxate, Octisalate, Oxybenzone, Avobenzone
10096-0299	Avon Elements	Octinoxate, Octisalate, Oxybenzone, Avobenzone
10096-0185	Clearskin Professional	OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
60541-0706	Moisturizing Tint	Octinoxate, Octisalate, Oxybenzone, Avobenzone
10096-0178	Solutions	OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
67879-302	SUN THERAPE FACE	OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE
67879-305	SUN THERAPE PRO SPORT FACE AND BODY	OCTINOXATE, OCTISALATE, OXYBENZONE, AVOBENZONE