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BOTANICAL PURE PACT - 51346-015-01 - (TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE)

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Drug Information of BOTANICAL PURE PACT

Product NDC: 51346-015
Proprietary Name: BOTANICAL PURE PACT
Non Proprietary Name: TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
Active Ingredient(s): .4; .62; .2    g/10g; g/10g; g/10g & nbsp;   TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
Administration Route(s): TOPICAL
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of BOTANICAL PURE PACT

Product NDC: 51346-015
Labeler Name: NATURE REPUBLIC CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120201

Package Information of BOTANICAL PURE PACT

Package NDC: 51346-015-01
Package Description: 10 g in 1 CARTON (51346-015-01)

NDC Information of BOTANICAL PURE PACT

NDC Code 51346-015-01
Proprietary Name BOTANICAL PURE PACT
Package Description 10 g in 1 CARTON (51346-015-01)
Product NDC 51346-015
Product Type Name HUMAN OTC DRUG
Non Proprietary Name TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
Dosage Form Name POWDER
Route Name TOPICAL
Start Marketing Date 20120201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name NATURE REPUBLIC CO., LTD.
Substance Name OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number .4; .62; .2
Strength Unit g/10g; g/10g; g/10g
Pharmaceutical Classes

Complete Information of BOTANICAL PURE PACT


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