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AMOREPACIFIC - 43419-501-11 - (OCTINOXATE and TITANIUM DIOXIDE)

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Drug Information of AMOREPACIFIC

Product NDC: 43419-501
Proprietary Name: AMOREPACIFIC
Non Proprietary Name: OCTINOXATE and TITANIUM DIOXIDE
Active Ingredient(s): 2.5; 1.05    mL/50mL; mL/50mL & nbsp;   OCTINOXATE and TITANIUM DIOXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of AMOREPACIFIC

Product NDC: 43419-501
Labeler Name: AMOREPACIFIC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110601

Package Information of AMOREPACIFIC

Package NDC: 43419-501-11
Package Description: 1 mL in 1 POUCH (43419-501-11)

NDC Information of AMOREPACIFIC

NDC Code 43419-501-11
Proprietary Name AMOREPACIFIC
Package Description 1 mL in 1 POUCH (43419-501-11)
Product NDC 43419-501
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE and TITANIUM DIOXIDE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110601
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name AMOREPACIFIC
Substance Name OCTINOXATE; TITANIUM DIOXIDE
Strength Number 2.5; 1.05
Strength Unit mL/50mL; mL/50mL
Pharmaceutical Classes

Complete Information of AMOREPACIFIC


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