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Olay Complete All Day - 37000-281-12 - (Avobenzone, Homosalate, Octisalate, and Octocrylene)

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Drug Information of Olay Complete All Day

Product NDC: 37000-281
Proprietary Name: Olay Complete All Day
Non Proprietary Name: Avobenzone, Homosalate, Octisalate, and Octocrylene
Active Ingredient(s): .03; .03; .05; .026    mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   Avobenzone, Homosalate, Octisalate, and Octocrylene
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Olay Complete All Day

Product NDC: 37000-281
Labeler Name: Procter & Gamble Manufacturing Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120401

Package Information of Olay Complete All Day

Package NDC: 37000-281-12
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (37000-281-12) > 120 mL in 1 BOTTLE, PLASTIC

NDC Information of Olay Complete All Day

NDC Code 37000-281-12
Proprietary Name Olay Complete All Day
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (37000-281-12) > 120 mL in 1 BOTTLE, PLASTIC
Product NDC 37000-281
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Homosalate, Octisalate, and Octocrylene
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120401
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Procter & Gamble Manufacturing Company
Substance Name AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
Strength Number .03; .03; .05; .026
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Olay Complete All Day


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