Product NDC: | 48871-002 |
Proprietary Name: | Hannaford Hand Sanitizer |
Non Proprietary Name: | Ethyl alcohol |
Active Ingredient(s): | 4.65 mL/7.5mL & nbsp; Ethyl alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 48871-002 |
Labeler Name: | Health-Tech, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100331 |
Package NDC: | 48871-002-01 |
Package Description: | 6 CARTON in 1 CASE (48871-002-01) > 12 BLISTER PACK in 1 CARTON > 1 BOTTLE, SPRAY in 1 BLISTER PACK > 7.5 mL in 1 BOTTLE, SPRAY |
NDC Code | 48871-002-01 |
Proprietary Name | Hannaford Hand Sanitizer |
Package Description | 6 CARTON in 1 CASE (48871-002-01) > 12 BLISTER PACK in 1 CARTON > 1 BOTTLE, SPRAY in 1 BLISTER PACK > 7.5 mL in 1 BOTTLE, SPRAY |
Product NDC | 48871-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ethyl alcohol |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20100331 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Health-Tech, Inc. |
Substance Name | ALCOHOL |
Strength Number | 4.65 |
Strength Unit | mL/7.5mL |
Pharmaceutical Classes |