NDC 42952-101

I-MAX EXCELLENCE

Avobenzone Octinoxate Oxybenzone

I-MAX EXCELLENCE is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Maxlife Usa, Inc.. The primary component is Avobenzone; Octinoxate; Oxybenzone.

• Product ID: 42952-101_98fc49ff-0f37-48e8-99e7-4060418c5aca
• NDC: 42952-101
• Product Type: Human Otc Drug
• Proprietary Name: I-MAX EXCELLENCE
• Generic Name: Avobenzone Octinoxate Oxybenzone
• Dosage Form: Lotion
• Route of Administration: TOPICAL
• Marketing Start Date: 2012-03-15
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part352
• Labeler Name: MAXLIFE USA, INC.
• Substance Name: AVOBENZONE; OCTINOXATE; OXYBENZONE
• Active Ingredient Strength: 3 g/100mL; g/100mL; g/100mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 42952-101-12

59 mL in 1 BOTTLE (42952-101-12)

• Marketing Start Date: 2012-03-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 42952-101-22 [42952010122]

I-MAX EXCELLENCE LOTION

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-06-01
• Marketing End Date: 2018-10-09

NDC 42952-101-12 [42952010112]

I-MAX EXCELLENCE LOTION

• Marketing Category: OTC monograph not final
• Application Number: part352
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-03-15

Drug Details

Active Ingredients

Ingredient	Strength
AVOBENZONE	2.5 g/100mL

OpenFDA Data

• SPL SET ID: 0a654c5f-32c0-4599-91c3-1f17877aa8cb
• Manufacturer:
  • MAXLIFE USA, INC.
• UNII:
  • G63QQF2NOX
  • 95OOS7VE0Y
  • 4Y5P7MUD51

NDC Crossover Matching brand name "I-MAX EXCELLENCE" or generic name "Avobenzone Octinoxate Oxybenzone"

NDC	Brand Name	Generic Name
42952-101	I-MAX EXCELLENCE	AVOBENZONE OCTINOXATE OXYBENZONE
63550-120	DAY C	AVOBENZONE OCTINOXATE OXYBENZONE
63550-192	Soothing Day SPF 15	AVOBENZONE OCTINOXATE OXYBENZONE