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GOODSENSE ANTIBACTERIAL MOISTURIZING
GOODSENSE ANTIBACTERIAL MOISTURIZING - 75981-004-59 - (BENZALKONIUM CHLORIDE)
Drug Information of GOODSENSE ANTIBACTERIAL MOISTURIZING
| Product NDC: | 75981-004 |
| Proprietary Name: | GOODSENSE ANTIBACTERIAL MOISTURIZING |
| Non Proprietary Name: | BENZALKONIUM CHLORIDE |
| Active Ingredient(s): | .115 g/1001 & nbsp; BENZALKONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | FILM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GOODSENSE ANTIBACTERIAL MOISTURIZING
| Product NDC: | 75981-004 |
| Labeler Name: | GEISS, DESTIN AND DUNN, INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110221 |
Package Information of GOODSENSE ANTIBACTERIAL MOISTURIZING
| Package NDC: | 75981-004-59 |
| Package Description: | 40 FILM in 1 BOTTLE (75981-004-59) |
NDC Information of GOODSENSE ANTIBACTERIAL MOISTURIZING
| NDC Code | 75981-004-59 |
| Proprietary Name | GOODSENSE ANTIBACTERIAL MOISTURIZING |
| Package Description | 40 FILM in 1 BOTTLE (75981-004-59) |
| Product NDC | 75981-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZALKONIUM CHLORIDE |
| Dosage Form Name | FILM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110221 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GEISS, DESTIN AND DUNN, INC. |
| Substance Name | BENZALKONIUM CHLORIDE |
| Strength Number | .115 |
| Strength Unit | g/1001 |
| Pharmaceutical Classes |
