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Theradent
Theradent - 52389-118-08 - (Calcium acetate, potassium nitrate, potassium phosphate, sodium fluoride)
Drug Information of Theradent
| Product NDC: | 52389-118 |
| Proprietary Name: | Theradent |
| Non Proprietary Name: | Calcium acetate, potassium nitrate, potassium phosphate, sodium fluoride |
| Active Ingredient(s): | 1; 6; 1; 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Calcium acetate, potassium nitrate, potassium phosphate, sodium fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Theradent
| Product NDC: | 52389-118 |
| Labeler Name: | Alva-Amco Pharmacal Companies, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20060717 |
Package Information of Theradent
| Package NDC: | 52389-118-08 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (52389-118-08) > 237 mL in 1 BOTTLE, PLASTIC (52389-118-01) |
NDC Information of Theradent
| NDC Code | 52389-118-08 |
| Proprietary Name | Theradent |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (52389-118-08) > 237 mL in 1 BOTTLE, PLASTIC (52389-118-01) |
| Product NDC | 52389-118 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Calcium acetate, potassium nitrate, potassium phosphate, sodium fluoride |
| Dosage Form Name | MOUTHWASH |
| Route Name | ORAL |
| Start Marketing Date | 20060717 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Alva-Amco Pharmacal Companies, Inc. |
| Substance Name | CALCIUM ACETATE; POTASSIUM NITRATE; POTASSIUM PHOSPHATE, DIBASIC; SODIUM FLUORIDE |
| Strength Number | 1; 6; 1; 3 |
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharmaceutical Classes |
