| Product NDC: | 40061-990 |
| Proprietary Name: | Patricks Sunscreen |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octocrylene, Oxybenzone |
| Active Ingredient(s): | 2; 7.25; 9.75; 3 g/100g; g/100g; g/100g; g/100g & nbsp; Avobenzone, Octinoxate, Octocrylene, Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 40061-990 |
| Labeler Name: | O.P. Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110428 |
| Package NDC: | 40061-990-08 |
| Package Description: | 8 PACKET in 1 CELLO PACK (40061-990-08) > 8.75 g in 1 PACKET (40061-990-10) |
| NDC Code | 40061-990-08 |
| Proprietary Name | Patricks Sunscreen |
| Package Description | 8 PACKET in 1 CELLO PACK (40061-990-08) > 8.75 g in 1 PACKET (40061-990-10) |
| Product NDC | 40061-990 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octocrylene, Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110428 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | O.P. Products, Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 2; 7.25; 9.75; 3 |
| Strength Unit | g/100g; g/100g; g/100g; g/100g |
| Pharmaceutical Classes |