| 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 |