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Tahitian Noni - 44717-536-02 - (Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone)

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Drug Information of Tahitian Noni

Product NDC: 44717-536
Proprietary Name: Tahitian Noni
Non Proprietary Name: Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone
Active Ingredient(s): 2; 6.5; 7; 5; 3    mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp;   Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Tahitian Noni

Product NDC: 44717-536
Labeler Name: Wasatch Product Development
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100628

Package Information of Tahitian Noni

Package NDC: 44717-536-02
Package Description: 1 BOTTLE in 1 BOX (44717-536-02) > 200 mL in 1 BOTTLE (44717-536-01)

NDC Information of Tahitian Noni

NDC Code 44717-536-02
Proprietary Name Tahitian Noni
Package Description 1 BOTTLE in 1 BOX (44717-536-02) > 200 mL in 1 BOTTLE (44717-536-01)
Product NDC 44717-536
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20100628
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Wasatch Product Development
Substance Name AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 2; 6.5; 7; 5; 3
Strength Unit mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Tahitian Noni


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