Home
>
National Drug Code (NDC)
>
AVAPTA
AVAPTA - 76332-002-01 - (ALLANTOIN, HEXYLRESORCINOL, MENTHOL, WHITE CAMPHOR)
Drug Information of AVAPTA
| Product NDC: | 76332-002 |
| Proprietary Name: | AVAPTA |
| Non Proprietary Name: | ALLANTOIN, HEXYLRESORCINOL, MENTHOL, WHITE CAMPHOR |
| Active Ingredient(s): | 5; 9; 1; 4 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; ALLANTOIN, HEXYLRESORCINOL, MENTHOL, WHITE CAMPHOR |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AVAPTA
| Product NDC: | 76332-002 |
| Labeler Name: | Neel Products LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120816 |
Package Information of AVAPTA
| Package NDC: | 76332-002-01 |
| Package Description: | 118 mL in 1 BOTTLE, SPRAY (76332-002-01) |
NDC Information of AVAPTA
| NDC Code | 76332-002-01 |
| Proprietary Name | AVAPTA |
| Package Description | 118 mL in 1 BOTTLE, SPRAY (76332-002-01) |
| Product NDC | 76332-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALLANTOIN, HEXYLRESORCINOL, MENTHOL, WHITE CAMPHOR |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20120816 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Neel Products LLC |
| Substance Name | ALLANTOIN; CAMPHOR (NATURAL); HEXYLRESORCINOL; MENTHOL |
| Strength Number | 5; 9; 1; 4 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
