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SCRUBS Solar Guard Sunscreen Wipe - 51239-0912-1 - (Sunscreen Wipe)

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Drug Information of SCRUBS Solar Guard Sunscreen Wipe

Product NDC: 51239-0912
Proprietary Name: SCRUBS Solar Guard Sunscreen Wipe
Non Proprietary Name: Sunscreen Wipe
Active Ingredient(s): 20; 75; 40; 50    g/856mL; g/856mL; g/856mL; g/856mL & nbsp;   Sunscreen Wipe
Administration Route(s): TOPICAL
Dosage Form(s): CLOTH
Coding System: National Drug Codes(NDC)

Labeler Information of SCRUBS Solar Guard Sunscreen Wipe

Product NDC: 51239-0912
Labeler Name: ITW Dymon
Product Type: HUMAN OTC DRUG
FDA Application Number: part352
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100301

Package Information of SCRUBS Solar Guard Sunscreen Wipe

Package NDC: 51239-0912-1
Package Description: 9 mL in 1 PACKET (51239-0912-1)

NDC Information of SCRUBS Solar Guard Sunscreen Wipe

NDC Code 51239-0912-1
Proprietary Name SCRUBS Solar Guard Sunscreen Wipe
Package Description 9 mL in 1 PACKET (51239-0912-1)
Product NDC 51239-0912
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sunscreen Wipe
Dosage Form Name CLOTH
Route Name TOPICAL
Start Marketing Date 20100301
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name ITW Dymon
Substance Name HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE
Strength Number 20; 75; 40; 50
Strength Unit g/856mL; g/856mL; g/856mL; g/856mL
Pharmaceutical Classes

Complete Information of SCRUBS Solar Guard Sunscreen Wipe


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