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Lumene Vitamin C Pure Radiance Day - 67692-081-01 - (AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE)

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Drug Information of Lumene Vitamin C Pure Radiance Day

Product NDC: 67692-081
Proprietary Name: Lumene Vitamin C Pure Radiance Day
Non Proprietary Name: AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE
Active Ingredient(s): 3; 7.5; 4; 5    mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Lumene Vitamin C Pure Radiance Day

Product NDC: 67692-081
Labeler Name: LUMENE OY
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20101122

Package Information of Lumene Vitamin C Pure Radiance Day

Package NDC: 67692-081-01
Package Description: 15 mL in 1 JAR (67692-081-01)

NDC Information of Lumene Vitamin C Pure Radiance Day

NDC Code 67692-081-01
Proprietary Name Lumene Vitamin C Pure Radiance Day
Package Description 15 mL in 1 JAR (67692-081-01)
Product NDC 67692-081
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20101122
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name LUMENE OY
Substance Name AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 3; 7.5; 4; 5
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Lumene Vitamin C Pure Radiance Day


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