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Version X Scalp Tonic
Version X Scalp Tonic - 58069-010-01 - (Allantoin)
Drug Information of Version X Scalp Tonic
| Product NDC: | 58069-010 |
| Proprietary Name: | Version X Scalp Tonic |
| Non Proprietary Name: | Allantoin |
| Active Ingredient(s): | .625 mg/125mL & nbsp; Allantoin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Version X Scalp Tonic
| Product NDC: | 58069-010 |
| Labeler Name: | CHRISTLTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130201 |
Package Information of Version X Scalp Tonic
| Package NDC: | 58069-010-01 |
| Package Description: | 125 mL in 1 CARTON (58069-010-01) |
NDC Information of Version X Scalp Tonic
| NDC Code | 58069-010-01 |
| Proprietary Name | Version X Scalp Tonic |
| Package Description | 125 mL in 1 CARTON (58069-010-01) |
| Product NDC | 58069-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Allantoin |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CHRISTLTD |
| Substance Name | ALLANTOIN |
| Strength Number | .625 |
| Strength Unit | mg/125mL |
| Pharmaceutical Classes |
