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Neova DNA Damage Control - Active - 62362-129-01 - (Zinc Oxide, Octinoxate, Octisalate)

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Drug Information of Neova DNA Damage Control - Active

Product NDC: 62362-129
Proprietary Name: Neova DNA Damage Control - Active
Non Proprietary Name: Zinc Oxide, Octinoxate, Octisalate
Active Ingredient(s): 7.5; 3; 8    mL/100mL; mL/100mL; mL/100mL & nbsp;   Zinc Oxide, Octinoxate, Octisalate
Administration Route(s): TOPICAL
Dosage Form(s): EMULSION
Coding System: National Drug Codes(NDC)

Labeler Information of Neova DNA Damage Control - Active

Product NDC: 62362-129
Labeler Name: PhotoMedex, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120105

Package Information of Neova DNA Damage Control - Active

Package NDC: 62362-129-01
Package Description: 1 TUBE in 1 BOX (62362-129-01) > 89 mL in 1 TUBE (62362-129-89)

NDC Information of Neova DNA Damage Control - Active

NDC Code 62362-129-01
Proprietary Name Neova DNA Damage Control - Active
Package Description 1 TUBE in 1 BOX (62362-129-01) > 89 mL in 1 TUBE (62362-129-89)
Product NDC 62362-129
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Zinc Oxide, Octinoxate, Octisalate
Dosage Form Name EMULSION
Route Name TOPICAL
Start Marketing Date 20120105
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name PhotoMedex, Inc.
Substance Name OCTINOXATE; OCTISALATE; ZINC OXIDE
Strength Number 7.5; 3; 8
Strength Unit mL/100mL; mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of Neova DNA Damage Control - Active


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