Home
>
National Drug Code (NDC)
>
Rocky Mountain Sunscreen
Rocky Mountain Sunscreen - 59260-135-09 - (Octinoxate, octisalate, octocrylene, titanium dioxide)
Drug Information of Rocky Mountain Sunscreen
| Product NDC: | 59260-135 |
| Proprietary Name: | Rocky Mountain Sunscreen |
| Non Proprietary Name: | Octinoxate, octisalate, octocrylene, titanium dioxide |
| Active Ingredient(s): | 7.5; 5; 10; 1.3 L/100L; L/100L; L/100L; L/100L & nbsp; Octinoxate, octisalate, octocrylene, titanium dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rocky Mountain Sunscreen
| Product NDC: | 59260-135 |
| Labeler Name: | Creative Cosmetics Inc. dba CCI |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100519 |
Package Information of Rocky Mountain Sunscreen
| Package NDC: | 59260-135-09 |
| Package Description: | 3.78 L in 1 JUG (59260-135-09) |
NDC Information of Rocky Mountain Sunscreen
| NDC Code | 59260-135-09 |
| Proprietary Name | Rocky Mountain Sunscreen |
| Package Description | 3.78 L in 1 JUG (59260-135-09) |
| Product NDC | 59260-135 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, octisalate, octocrylene, titanium dioxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100519 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Creative Cosmetics Inc. dba CCI |
| Substance Name | OCTINOXATE; OCTISALATE; OCTOCRYLENE; TITANIUM DIOXIDE |
| Strength Number | 7.5; 5; 10; 1.3 |
| Strength Unit | L/100L; L/100L; L/100L; L/100L |
| Pharmaceutical Classes |
