Home
>
National Drug Code (NDC)
>
Sunscreen Wipe
Sunscreen Wipe - 52648-6175-1 - (HOMOSALATE OCTINOXATE OCTISALATE OXYBENZONE)
Drug Information of Sunscreen Wipe
| Product NDC: | 52648-6175 |
| Proprietary Name: | Sunscreen Wipe |
| Non Proprietary Name: | HOMOSALATE OCTINOXATE OCTISALATE OXYBENZONE |
| Active Ingredient(s): | 20; 75; 40; 50 g/856mL; g/856mL; g/856mL; g/856mL & nbsp; HOMOSALATE OCTINOXATE OCTISALATE OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CLOTH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunscreen Wipe
| Product NDC: | 52648-6175 |
| Labeler Name: | KGP Products, Inc. (dba PREMIER) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100928 |
Package Information of Sunscreen Wipe
| Package NDC: | 52648-6175-1 |
| Package Description: | 9 mL in 1 PACKET (52648-6175-1) |
NDC Information of Sunscreen Wipe
| NDC Code | 52648-6175-1 |
| Proprietary Name | Sunscreen Wipe |
| Package Description | 9 mL in 1 PACKET (52648-6175-1) |
| Product NDC | 52648-6175 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HOMOSALATE OCTINOXATE OCTISALATE OXYBENZONE |
| Dosage Form Name | CLOTH |
| Route Name | TOPICAL |
| Start Marketing Date | 20100928 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | KGP Products, Inc. (dba PREMIER) |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 20; 75; 40; 50 |
| Strength Unit | g/856mL; g/856mL; g/856mL; g/856mL |
| Pharmaceutical Classes |
