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Face and Body Sunscreen - 67510-0081-5 - (Octinoxate and Titanium dioxide)

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Drug Information of Face and Body Sunscreen

Product NDC: 67510-0081
Proprietary Name: Face and Body Sunscreen
Non Proprietary Name: Octinoxate and Titanium dioxide
Active Ingredient(s): 7; 2.8    g/100mL; g/100mL & nbsp;   Octinoxate and Titanium dioxide
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Face and Body Sunscreen

Product NDC: 67510-0081
Labeler Name: Kareway Product, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130124

Package Information of Face and Body Sunscreen

Package NDC: 67510-0081-5
Package Description: 100 mL in 1 TUBE (67510-0081-5)

NDC Information of Face and Body Sunscreen

NDC Code 67510-0081-5
Proprietary Name Face and Body Sunscreen
Package Description 100 mL in 1 TUBE (67510-0081-5)
Product NDC 67510-0081
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate and Titanium dioxide
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20130124
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Kareway Product, Inc.
Substance Name OCTINOXATE; TITANIUM DIOXIDE
Strength Number 7; 2.8
Strength Unit g/100mL; g/100mL
Pharmaceutical Classes

Complete Information of Face and Body Sunscreen


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