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Guerlain Super Aqua-Day - 49817-0021-1 - (OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, OCTOCRYLENE, SULISOBENZONE)

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Drug Information of Guerlain Super Aqua-Day

Product NDC: 49817-0021
Proprietary Name: Guerlain Super Aqua-Day
Non Proprietary Name: OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, OCTOCRYLENE, SULISOBENZONE
Active Ingredient(s): 7.4; 2; 3; .5; 2.4    mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, OCTOCRYLENE, SULISOBENZONE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Guerlain Super Aqua-Day

Product NDC: 49817-0021
Labeler Name: Guerlain S.A.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100617

Package Information of Guerlain Super Aqua-Day

Package NDC: 49817-0021-1
Package Description: 40 mL in 1 BOTTLE (49817-0021-1)

NDC Information of Guerlain Super Aqua-Day

NDC Code 49817-0021-1
Proprietary Name Guerlain Super Aqua-Day
Package Description 40 mL in 1 BOTTLE (49817-0021-1)
Product NDC 49817-0021
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, OCTOCRYLENE, SULISOBENZONE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20100617
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Guerlain S.A.
Substance Name OCTINOXATE; OCTOCRYLENE; OXYBENZONE; SULISOBENZONE; TITANIUM DIOXIDE
Strength Number 7.4; 2; 3; .5; 2.4
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Guerlain Super Aqua-Day


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