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