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UVA/UVB SPF 15 - 14222-2022-2 - (Octinoxate, Zinc Oxide)

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Drug Information of UVA/UVB SPF 15

Product NDC: 14222-2022
Proprietary Name: UVA/UVB SPF 15
Non Proprietary Name: Octinoxate, Zinc Oxide
Active Ingredient(s): 7.5; 3.4    mL/100mL; mL/100mL & nbsp;   Octinoxate, Zinc Oxide
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of UVA/UVB SPF 15

Product NDC: 14222-2022
Labeler Name: Rodan & Fields LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110603

Package Information of UVA/UVB SPF 15

Package NDC: 14222-2022-2
Package Description: 1 BOTTLE in 1 BOX (14222-2022-2) > 50 mL in 1 BOTTLE (14222-2022-1)

NDC Information of UVA/UVB SPF 15

NDC Code 14222-2022-2
Proprietary Name UVA/UVB SPF 15
Package Description 1 BOTTLE in 1 BOX (14222-2022-2) > 50 mL in 1 BOTTLE (14222-2022-1)
Product NDC 14222-2022
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Octinoxate, Zinc Oxide
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20110603
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Rodan & Fields LLC.
Substance Name OCTINOXATE; ZINC OXIDE
Strength Number 7.5; 3.4
Strength Unit mL/100mL; mL/100mL
Pharmaceutical Classes

Complete Information of UVA/UVB SPF 15


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