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RED ORANGE SUN PACT - 76214-037-01 - (OCTINOXATE)

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Drug Information of RED ORANGE SUN PACT

Product NDC: 76214-037
Proprietary Name: RED ORANGE SUN PACT
Non Proprietary Name: OCTINOXATE
Active Ingredient(s): .66; .29; .27    g/9.5g; g/9.5g; g/9.5g & nbsp;   OCTINOXATE
Administration Route(s): CUTANEOUS
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of RED ORANGE SUN PACT

Product NDC: 76214-037
Labeler Name: SKINFOOD CO., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110301

Package Information of RED ORANGE SUN PACT

Package NDC: 76214-037-01
Package Description: 9.5 g in 1 CARTON (76214-037-01)

NDC Information of RED ORANGE SUN PACT

NDC Code 76214-037-01
Proprietary Name RED ORANGE SUN PACT
Package Description 9.5 g in 1 CARTON (76214-037-01)
Product NDC 76214-037
Product Type Name HUMAN OTC DRUG
Non Proprietary Name OCTINOXATE
Dosage Form Name POWDER
Route Name CUTANEOUS
Start Marketing Date 20110301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name SKINFOOD CO., LTD.
Substance Name OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Strength Number .66; .29; .27
Strength Unit g/9.5g; g/9.5g; g/9.5g
Pharmaceutical Classes

Complete Information of RED ORANGE SUN PACT


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