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Whitening Foaming
Whitening Foaming - 75902-1001-1 - (Sodium fluoride)
Drug Information of Whitening Foaming
| Product NDC: | 75902-1001 |
| Proprietary Name: | Whitening Foaming |
| Non Proprietary Name: | Sodium fluoride |
| Active Ingredient(s): | .0005; .001 mL/mL; mL/mL & nbsp; Sodium fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Whitening Foaming
| Product NDC: | 75902-1001 |
| Labeler Name: | Dio Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101217 |
Package Information of Whitening Foaming
| Package NDC: | 75902-1001-1 |
| Package Description: | 50 mL in 1 BOTTLE, PUMP (75902-1001-1) |
NDC Information of Whitening Foaming
| NDC Code | 75902-1001-1 |
| Proprietary Name | Whitening Foaming |
| Package Description | 50 mL in 1 BOTTLE, PUMP (75902-1001-1) |
| Product NDC | 75902-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Sodium fluoride |
| Dosage Form Name | MOUTHWASH |
| Route Name | DENTAL |
| Start Marketing Date | 20101217 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Dio Corporation |
| Substance Name | ALLANTOIN; SODIUM FLUORIDE |
| Strength Number | .0005; .001 |
| Strength Unit | mL/mL; mL/mL |
| Pharmaceutical Classes |
