Product NDC: | 10056-700 |
Proprietary Name: | Peter Island Sunscreen |
Non Proprietary Name: | OCTOCRYLENE OXYBENZONE ZINC OXIDE |
Active Ingredient(s): | 5; 2; 3.9 g/100g; g/100g; g/100g & nbsp; OCTOCRYLENE OXYBENZONE ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10056-700 |
Labeler Name: | ACCESS BUSINESS GROUP INTERNATIONAL LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121120 |
Package NDC: | 10056-700-13 |
Package Description: | 113 g in 1 BOTTLE, PLASTIC (10056-700-13) |
NDC Code | 10056-700-13 |
Proprietary Name | Peter Island Sunscreen |
Package Description | 113 g in 1 BOTTLE, PLASTIC (10056-700-13) |
Product NDC | 10056-700 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTOCRYLENE OXYBENZONE ZINC OXIDE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20121120 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | ACCESS BUSINESS GROUP INTERNATIONAL LLC |
Substance Name | OCTOCRYLENE; OXYBENZONE; ZINC OXIDE |
Strength Number | 5; 2; 3.9 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmaceutical Classes |