Home
>
National Drug Code (NDC)
>
EQUALINE
EQUALINE - 41163-358-12 - (DIMETHICONE)
Drug Information of EQUALINE
| Product NDC: | 41163-358 |
| Proprietary Name: | EQUALINE |
| Non Proprietary Name: | DIMETHICONE |
| Active Ingredient(s): | 13 mg/mL & nbsp; DIMETHICONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EQUALINE
| Product NDC: | 41163-358 |
| Labeler Name: | SUPERVALU INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130115 |
Package Information of EQUALINE
| Package NDC: | 41163-358-12 |
| Package Description: | 354 mL in 1 BOTTLE, PLASTIC (41163-358-12) |
NDC Information of EQUALINE
| NDC Code | 41163-358-12 |
| Proprietary Name | EQUALINE |
| Package Description | 354 mL in 1 BOTTLE, PLASTIC (41163-358-12) |
| Product NDC | 41163-358 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIMETHICONE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130115 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SUPERVALU INC. |
| Substance Name | DIMETHICONE |
| Strength Number | 13 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
