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NDC 49035-0569-99 4X Medicated Toothache and Gum Gel .13; 20; .5; .15 g/100g; g/100g; g/100g; g/100g Details
4X Medicated Toothache and Gum Gel .13; 20; .5; .15 g/100g; g/100g; g/100g; g/100g
4X Medicated Toothache and Gum Gel is a ORAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by Walmart. The primary component is BENZALKONIUM CHLORIDE; BENZOCAINE; MENTHOL; ZINC CHLORIDE.
Product Information
| NDC | 49035-0569 |
|---|---|
| Product ID | 49035-569_f2f22e2d-ba00-d9a5-e053-2a95a90ab970 |
| 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 | 4X 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 | .13; 20; .5; .15 |
| Active Ingredient Units | g/100g; g/100g; g/100g; g/100g |
| Substance Name | BENZALKONIUM CHLORIDE; BENZOCAINE; MENTHOL; ZINC CHLORIDE |
| Labeler Name | Walmart |
| 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 49035-0569-99 (49035056999)
| NDC Package Code | 49035-569-99 |
|---|---|
| Billing NDC | 49035056999 |
| Package | 1 g in 1 TUBE (49035-569-99) |
| Marketing Start Date | 2020-05-18 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |