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SunDrops 75
SunDrops 75 - 63621-356-20 - (Alcohol)
Drug Information of SunDrops 75
| Product NDC: | 63621-356 |
| Proprietary Name: | SunDrops 75 |
| Non Proprietary Name: | Alcohol |
| Active Ingredient(s): | .6 mL/mL & nbsp; Alcohol |
| Administration Route(s): | CUTANEOUS |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SunDrops 75
| Product NDC: | 63621-356 |
| Labeler Name: | Sunburst Chemicals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20091014 |
Package Information of SunDrops 75
| Package NDC: | 63621-356-20 |
| Package Description: | 1000 mL in 1 BAG (63621-356-20) |
NDC Information of SunDrops 75
| NDC Code | 63621-356-20 |
| Proprietary Name | SunDrops 75 |
| Package Description | 1000 mL in 1 BAG (63621-356-20) |
| Product NDC | 63621-356 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Alcohol |
| Dosage Form Name | GEL |
| Route Name | CUTANEOUS |
| Start Marketing Date | 20091014 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Sunburst Chemicals, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | .6 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
