Product NDC: | 15304-4085 |
Proprietary Name: | Mastic Dent |
Non Proprietary Name: | Sodium Fluoride, Eucalyptol, Thymol and Menthol |
Active Ingredient(s): | .92; .42; .25; .64 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Sodium Fluoride, Eucalyptol, Thymol and Menthol |
Administration Route(s): | DENTAL; ORAL |
Dosage Form(s): | MOUTHWASH |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 15304-4085 |
Labeler Name: | Chia Gi LTD |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part356 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20051122 |
Package NDC: | 15304-4085-1 |
Package Description: | 400 mL in 1 BOTTLE, PLASTIC (15304-4085-1) |
NDC Code | 15304-4085-1 |
Proprietary Name | Mastic Dent |
Package Description | 400 mL in 1 BOTTLE, PLASTIC (15304-4085-1) |
Product NDC | 15304-4085 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sodium Fluoride, Eucalyptol, Thymol and Menthol |
Dosage Form Name | MOUTHWASH |
Route Name | DENTAL; ORAL |
Start Marketing Date | 20051122 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Chia Gi LTD |
Substance Name | EUCALYPTOL; MENTHOL; SODIUM FLUORIDE; THYMOL |
Strength Number | .92; .42; .25; .64 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |