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EQUALINE
EQUALINE - 41163-621-11 - (SELENIUM SULFIDE)
Drug Information of EQUALINE
| Product NDC: | 41163-621 |
| Proprietary Name: | EQUALINE |
| Non Proprietary Name: | SELENIUM SULFIDE |
| Active Ingredient(s): | 10 mg/mL & nbsp; SELENIUM SULFIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EQUALINE
| Product NDC: | 41163-621 |
| Labeler Name: | SUPERVALU INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130610 |
Package Information of EQUALINE
| Package NDC: | 41163-621-11 |
| Package Description: | 325 mL in 1 BOTTLE, PLASTIC (41163-621-11) |
NDC Information of EQUALINE
| NDC Code | 41163-621-11 |
| Proprietary Name | EQUALINE |
| Package Description | 325 mL in 1 BOTTLE, PLASTIC (41163-621-11) |
| Product NDC | 41163-621 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SELENIUM SULFIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130610 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SUPERVALU INC. |
| Substance Name | SELENIUM SULFIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
