Product NDC: | 49852-200 |
Proprietary Name: | Suntan Lotion |
Non Proprietary Name: | OCTINOXATE OXYBENZONE TITANIUM DIOXIDE |
Active Ingredient(s): | 7; 6; 1 mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE OXYBENZONE TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49852-200 |
Labeler Name: | Tri-Coastal Design Company Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100228 |
Package NDC: | 49852-200-60 |
Package Description: | 60 mL in 1 TUBE (49852-200-60) |
NDC Code | 49852-200-60 |
Proprietary Name | Suntan Lotion |
Package Description | 60 mL in 1 TUBE (49852-200-60) |
Product NDC | 49852-200 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE OXYBENZONE TITANIUM DIOXIDE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20100228 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Tri-Coastal Design Company Inc. |
Substance Name | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
Strength Number | 7; 6; 1 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |