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CRC Sunscreen Towel
CRC Sunscreen Towel - 66348-4105-1 - (Sunscreen Towel)
Drug Information of CRC Sunscreen Towel
| Product NDC: | 66348-4105 |
| Proprietary Name: | CRC Sunscreen Towel |
| Non Proprietary Name: | Sunscreen Towel |
| Active Ingredient(s): | 20; 75; 40; 50 g/856mL; g/856mL; g/856mL; g/856mL & nbsp; Sunscreen Towel |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CLOTH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CRC Sunscreen Towel
| Product NDC: | 66348-4105 |
| Labeler Name: | CRC Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100301 |
Package Information of CRC Sunscreen Towel
| Package NDC: | 66348-4105-1 |
| Package Description: | 9 mL in 1 PACKET (66348-4105-1) |
NDC Information of CRC Sunscreen Towel
| NDC Code | 66348-4105-1 |
| Proprietary Name | CRC Sunscreen Towel |
| Package Description | 9 mL in 1 PACKET (66348-4105-1) |
| Product NDC | 66348-4105 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sunscreen Towel |
| Dosage Form Name | CLOTH |
| Route Name | TOPICAL |
| Start Marketing Date | 20100301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CRC Industries, Inc. |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 20; 75; 40; 50 |
| Strength Unit | g/856mL; g/856mL; g/856mL; g/856mL |
| Pharmaceutical Classes |
