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MoistureWorx
MoistureWorx - 28109-020-06 - (petrolatum)
Drug Information of MoistureWorx
| Product NDC: | 28109-020 |
| Proprietary Name: | MoistureWorx |
| Non Proprietary Name: | petrolatum |
| Active Ingredient(s): | 36 mL/120mL & nbsp; petrolatum |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MoistureWorx
| Product NDC: | 28109-020 |
| Labeler Name: | DermWorx Incorporated |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080527 |
Package Information of MoistureWorx
| Package NDC: | 28109-020-06 |
| Package Description: | 6 CARTON in 1 CARTON (28109-020-06) > 1 BOTTLE in 1 CARTON (28109-020-01) > 120 mL in 1 BOTTLE |
NDC Information of MoistureWorx
| NDC Code | 28109-020-06 |
| Proprietary Name | MoistureWorx |
| Package Description | 6 CARTON in 1 CARTON (28109-020-06) > 1 BOTTLE in 1 CARTON (28109-020-01) > 120 mL in 1 BOTTLE |
| Product NDC | 28109-020 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | petrolatum |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20080527 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DermWorx Incorporated |
| Substance Name | PETROLATUM |
| Strength Number | 36 |
| Strength Unit | mL/120mL |
| Pharmaceutical Classes |
