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ICS PLATINUM - 75909-110-01 - (TITANIUM DIOXIDE)

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Drug Information of ICS PLATINUM

Product NDC: 75909-110
Proprietary Name: ICS PLATINUM
Non Proprietary Name: TITANIUM DIOXIDE
Active Ingredient(s): 2.69; .67    mL/35mL; mL/35mL & nbsp;   TITANIUM DIOXIDE
Administration Route(s): CUTANEOUS
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of ICS PLATINUM

Product NDC: 75909-110
Labeler Name: HANBUL COSMETICS CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100401

Package Information of ICS PLATINUM

Package NDC: 75909-110-01
Package Description: 35 mL in 1 CARTON (75909-110-01)

NDC Information of ICS PLATINUM

NDC Code 75909-110-01
Proprietary Name ICS PLATINUM
Package Description 35 mL in 1 CARTON (75909-110-01)
Product NDC 75909-110
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TITANIUM DIOXIDE
Dosage Form Name CREAM
Route Name CUTANEOUS
Start Marketing Date 20100401
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name HANBUL COSMETICS CO., LTD.
Substance Name TITANIUM DIOXIDE; ZINC OXIDE
Strength Number 2.69; .67
Strength Unit mL/35mL; mL/35mL
Pharmaceutical Classes

Complete Information of ICS PLATINUM


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