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DDF Ultra-Lite Oil-Free Moisturizing Dew - 37000-704-48 - (Avobenzone, Homosalate, Octisalate, and Octocrylene)

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Drug Information of DDF Ultra-Lite Oil-Free Moisturizing Dew

Product NDC: 37000-704
Proprietary Name: DDF Ultra-Lite Oil-Free Moisturizing Dew
Non Proprietary Name: Avobenzone, Homosalate, Octisalate, and Octocrylene
Active Ingredient(s): .03; .05; .05; .026    g/g; g/g; g/g; g/g & nbsp;   Avobenzone, Homosalate, Octisalate, and Octocrylene
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of DDF Ultra-Lite Oil-Free Moisturizing Dew

Product NDC: 37000-704
Labeler Name: Procter & Gamble Manufacturing Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121101

Package Information of DDF Ultra-Lite Oil-Free Moisturizing Dew

Package NDC: 37000-704-48
Package Description: 1 BOTTLE, PUMP in 1 CARTON (37000-704-48) > 48 g in 1 BOTTLE, PUMP

NDC Information of DDF Ultra-Lite Oil-Free Moisturizing Dew

NDC Code 37000-704-48
Proprietary Name DDF Ultra-Lite Oil-Free Moisturizing Dew
Package Description 1 BOTTLE, PUMP in 1 CARTON (37000-704-48) > 48 g in 1 BOTTLE, PUMP
Product NDC 37000-704
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Homosalate, Octisalate, and Octocrylene
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20121101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Procter & Gamble Manufacturing Company
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Strength Number .03; .05; .05; .026
Strength Unit g/g; g/g; g/g; g/g
Pharmaceutical Classes

Complete Information of DDF Ultra-Lite Oil-Free Moisturizing Dew


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