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NDC 51206-0311-01 Opal by Opalescence Sensitivity 50; 1.1 mg/g; mg/g Details
Opal by Opalescence Sensitivity 50; 1.1 mg/g; mg/g
Opal by Opalescence Sensitivity is a DENTAL GEL, DENTIFRICE in the HUMAN OTC DRUG category. It is labeled and distributed by Ultradent Products, Inc.. The primary component is POTASSIUM NITRATE; SODIUM FLUORIDE.
Product Information
| NDC | 51206-0311 |
|---|---|
| Product ID | 51206-311_86eb110a-1fe4-4a39-b227-ed6594089b1d |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Opal by Opalescence Sensitivity |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Potassium Nitrate and Sodium Fluoride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | GEL, DENTIFRICE |
| Route | DENTAL |
| Active Ingredient Strength | 50; 1.1 |
| Active Ingredient Units | mg/g; mg/g |
| Substance Name | POTASSIUM NITRATE; SODIUM FLUORIDE |
| Labeler Name | Ultradent Products, Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M022 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 51206-0311-01 (51206031101)
| NDC Package Code | 51206-311-01 |
|---|---|
| Billing NDC | 51206031101 |
| Package | 1 TUBE in 1 CARTON (51206-311-01) / 133 g in 1 TUBE |
| Marketing Start Date | 2023-11-19 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |