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 |