Product NDC: | 49757-002 |
Proprietary Name: | Rocky Mountain KIDS Broad Spectrum SPF 30 |
Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Active Ingredient(s): | 3; 10; 7.5; 5; 4 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49757-002 |
Labeler Name: | Rocky Mountain Sunscreen |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120427 |
Package NDC: | 49757-002-01 |
Package Description: | 3785.41 mL in 1 BOTTLE (49757-002-01) |
NDC Code | 49757-002-01 |
Proprietary Name | Rocky Mountain KIDS Broad Spectrum SPF 30 |
Package Description | 3785.41 mL in 1 BOTTLE (49757-002-01) |
Product NDC | 49757-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120427 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Rocky Mountain Sunscreen |
Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 3; 10; 7.5; 5; 4 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |