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OralLine
OralLine - 55873-002-01 - (SODIUM FLUORIDE)
Drug Information of OralLine
| Product NDC: | 55873-002 |
| Proprietary Name: | OralLine |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | .24 g/100g & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GEL, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OralLine
| Product NDC: | 55873-002 |
| Labeler Name: | J.M. Murray Center Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19660101 |
Package Information of OralLine
| Package NDC: | 55873-002-01 |
| Package Description: | 85 g in 1 TUBE (55873-002-01) |
NDC Information of OralLine
| NDC Code | 55873-002-01 |
| Proprietary Name | OralLine |
| Package Description | 85 g in 1 TUBE (55873-002-01) |
| Product NDC | 55873-002 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | GEL, DENTIFRICE |
| Route Name | ORAL |
| Start Marketing Date | 19660101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | J.M. Murray Center Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .24 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
