Product NDC: | 55301-001 |
Proprietary Name: | Exchange Select Sunscreen |
Non Proprietary Name: | OCTINOXATE OXYBENZONE |
Active Ingredient(s): | 2; 12; 5; 1.6; 3.5 g/100g; g/100g; g/100g; g/100g; g/100g & nbsp; OCTINOXATE OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55301-001 |
Labeler Name: | ARMY AND AIR FORCE EXCHANGE SERVICE |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121115 |
Package NDC: | 55301-001-13 |
Package Description: | 113 g in 1 BOTTLE, PLASTIC (55301-001-13) |
NDC Code | 55301-001-13 |
Proprietary Name | Exchange Select Sunscreen |
Package Description | 113 g in 1 BOTTLE, PLASTIC (55301-001-13) |
Product NDC | 55301-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE OXYBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20121115 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | ARMY AND AIR FORCE EXCHANGE SERVICE |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 2; 12; 5; 1.6; 3.5 |
Strength Unit | g/100g; g/100g; g/100g; g/100g; g/100g |
Pharmaceutical Classes |