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I-MAX EXCELLENCE - 42952-101-12 - (AVOBENZONE OCTINOXATE OXYBENZONE)

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Drug Information of I-MAX EXCELLENCE

Product NDC: 42952-101
Proprietary Name: I-MAX EXCELLENCE
Non Proprietary Name: AVOBENZONE OCTINOXATE OXYBENZONE
Active Ingredient(s): 2.5; 7.5; 5    g/100mL; g/100mL; g/100mL & nbsp;   AVOBENZONE OCTINOXATE OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of I-MAX EXCELLENCE

Product NDC: 42952-101
Labeler Name: MAXLIFE USA, INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120315

Package Information of I-MAX EXCELLENCE

Package NDC: 42952-101-12
Package Description: 59 mL in 1 BOTTLE (42952-101-12)

NDC Information of I-MAX EXCELLENCE

NDC Code 42952-101-12
Proprietary Name I-MAX EXCELLENCE
Package Description 59 mL in 1 BOTTLE (42952-101-12)
Product NDC 42952-101
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AVOBENZONE OCTINOXATE OXYBENZONE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120315
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name MAXLIFE USA, INC.
Substance Name AVOBENZONE; OCTINOXATE; OXYBENZONE
Strength Number 2.5; 7.5; 5
Strength Unit g/100mL; g/100mL; g/100mL
Pharmaceutical Classes

Complete Information of I-MAX EXCELLENCE


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