Product NDC: | 62802-218 |
Proprietary Name: | NO-AD 45 Sunscreen |
Non Proprietary Name: | avobenzone, homosalate, octisalate, oxybenzone |
Active Ingredient(s): | 2; 15; 5; 5 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; avobenzone, homosalate, octisalate, oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 62802-218 |
Labeler Name: | Sun & Skin Care Research, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120101 |
Package NDC: | 62802-218-16 |
Package Description: | 475 mL in 1 BOTTLE (62802-218-16) |
NDC Code | 62802-218-16 |
Proprietary Name | NO-AD 45 Sunscreen |
Package Description | 475 mL in 1 BOTTLE (62802-218-16) |
Product NDC | 62802-218 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | avobenzone, homosalate, octisalate, oxybenzone |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Sun & Skin Care Research, LLC |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OXYBENZONE |
Strength Number | 2; 15; 5; 5 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |