Product NDC: | 75981-007 |
Proprietary Name: | GOODSENSE MEDICATED PADS |
Non Proprietary Name: | WITCH HAZEL |
Active Ingredient(s): | .5 mL/mL & nbsp; WITCH HAZEL |
Administration Route(s): | RECTAL; TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75981-007 |
Labeler Name: | GEISS, DESTIN AND DUNN, INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part346 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110601 |
Package NDC: | 75981-007-47 |
Package Description: | 100 APPLICATOR in 1 JAR (75981-007-47) > 2.5 mL in 1 APPLICATOR |
NDC Code | 75981-007-47 |
Proprietary Name | GOODSENSE MEDICATED PADS |
Package Description | 100 APPLICATOR in 1 JAR (75981-007-47) > 2.5 mL in 1 APPLICATOR |
Product NDC | 75981-007 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | WITCH HAZEL |
Dosage Form Name | SOLUTION |
Route Name | RECTAL; TOPICAL |
Start Marketing Date | 20110601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | GEISS, DESTIN AND DUNN, INC. |
Substance Name | WITCH HAZEL |
Strength Number | .5 |
Strength Unit | mL/mL |
Pharmaceutical Classes |