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IOPE SUPER VITAL - 43419-371-42 - (TITANIUM DIOXIDE and OCTINOXATE)

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Drug Information of IOPE SUPER VITAL

Product NDC: 43419-371
Proprietary Name: IOPE SUPER VITAL
Non Proprietary Name: TITANIUM DIOXIDE and OCTINOXATE
Active Ingredient(s): 1.75; .35    mL/35mL; mL/35mL & nbsp;   TITANIUM DIOXIDE and OCTINOXATE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of IOPE SUPER VITAL

Product NDC: 43419-371
Labeler Name: AMOREPACIFIC
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110201

Package Information of IOPE SUPER VITAL

Package NDC: 43419-371-42
Package Description: 35 mL in 1 CONTAINER (43419-371-42)

NDC Information of IOPE SUPER VITAL

NDC Code 43419-371-42
Proprietary Name IOPE SUPER VITAL
Package Description 35 mL in 1 CONTAINER (43419-371-42)
Product NDC 43419-371
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TITANIUM DIOXIDE and OCTINOXATE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110201
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name AMOREPACIFIC
Substance Name OCTINOXATE; TITANIUM DIOXIDE
Strength Number 1.75; .35
Strength Unit mL/35mL; mL/35mL
Pharmaceutical Classes

Complete Information of IOPE SUPER VITAL


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