Product NDC: | 42485-007 |
Proprietary Name: | Lasting Results Moisturizer |
Non Proprietary Name: | octocrylene, octinoxate, oxybenzone,octisalate, avobenzone |
Active Ingredient(s): | 30; 75; 50; 100; 50 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; octocrylene, octinoxate, oxybenzone,octisalate, avobenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42485-007 |
Labeler Name: | Biopelle, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120501 |
Package NDC: | 42485-007-01 |
Package Description: | 75 mL in 1 BOTTLE, PLASTIC (42485-007-01) |
NDC Code | 42485-007-01 |
Proprietary Name | Lasting Results Moisturizer |
Package Description | 75 mL in 1 BOTTLE, PLASTIC (42485-007-01) |
Product NDC | 42485-007 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | octocrylene, octinoxate, oxybenzone,octisalate, avobenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120501 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Biopelle, Inc. |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 30; 75; 50; 100; 50 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |