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Ultra Protection SPF 40 - 68026-421-10 - (AVOBENZONE, HOMOSALATE, OCTISALATE, OXYBENZONE)

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Drug Information of Ultra Protection SPF 40

Product NDC: 68026-421
Proprietary Name: Ultra Protection SPF 40
Non Proprietary Name: AVOBENZONE, HOMOSALATE, OCTISALATE, OXYBENZONE
Active Ingredient(s): 3; 7; 5; 2    g/100g; g/100g; g/100g; g/100g & nbsp;   AVOBENZONE, HOMOSALATE, OCTISALATE, OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): STICK
Coding System: National Drug Codes(NDC)

Labeler Information of Ultra Protection SPF 40

Product NDC: 68026-421
Labeler Name: La Prairie, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110407

Package Information of Ultra Protection SPF 40

Package NDC: 68026-421-10
Package Description: 10 g in 1 PACKAGE (68026-421-10)

NDC Information of Ultra Protection SPF 40

NDC Code 68026-421-10
Proprietary Name Ultra Protection SPF 40
Package Description 10 g in 1 PACKAGE (68026-421-10)
Product NDC 68026-421
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AVOBENZONE, HOMOSALATE, OCTISALATE, OXYBENZONE
Dosage Form Name STICK
Route Name TOPICAL
Start Marketing Date 20110407
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name La Prairie, Inc.
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE
Strength Number 3; 7; 5; 2
Strength Unit g/100g; g/100g; g/100g; g/100g
Pharmaceutical Classes

Complete Information of Ultra Protection SPF 40


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