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NDC 69842-0693-39 3x Medicated Toothache and Gum Gel 20; .26; .15 g/100g; g/100g; g/100g Details
3x Medicated Toothache and Gum Gel 20; .26; .15 g/100g; g/100g; g/100g
3x Medicated Toothache and Gum Gel is a ORAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by CVS. The primary component is BENZOCAINE; MENTHOL, UNSPECIFIED FORM; ZINC CHLORIDE.
Product Information
| NDC | 69842-0693 |
|---|---|
| Product ID | 69842-693_f2f23228-fc35-2678-e053-2995a90a599d |
| 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 | 3x Medicated Toothache and Gum Gel |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Benzocaine |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | GEL |
| Route | ORAL |
| Active Ingredient Strength | 20; .26; .15 |
| Active Ingredient Units | g/100g; g/100g; g/100g |
| Substance Name | BENZOCAINE; MENTHOL, UNSPECIFIED FORM; ZINC CHLORIDE |
| Labeler Name | CVS |
| Pharmaceutical Class | Allergens [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part356 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 69842-0693-39 (69842069339)
| NDC Package Code | 69842-693-39 |
|---|---|
| Billing NDC | 69842069339 |
| Package | 1 TUBE in 1 CARTON (69842-693-39) / 7.1 g in 1 TUBE |
| Marketing Start Date | 2020-06-05 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |