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NDC 11822-0615-09 4X Medicated Severe Toothache and Gum Gel .13; 20; .5; .15 g/100g; g/100g; g/100g; g/100g Details
4X Medicated Severe Toothache and Gum Gel .13; 20; .5; .15 g/100g; g/100g; g/100g; g/100g
4X Medicated Severe Toothache and Gum Gel is a ORAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by Rite Aid. The primary component is BENZALKONIUM CHLORIDE; BENZOCAINE; MENTHOL; ZINC CHLORIDE.
Product Information
NDC | 11822-0615 |
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Product ID | 11822-0615_f2000136-02ee-19d3-e053-2995a90ab647 |
Associated GPIs | 42200015001810 |
GCN Sequence Number | 075590 |
GCN Sequence Number Description | budesonide SPRAY/PUMP 32 MCG NASAL |
HIC3 | Q7P |
HIC3 Description | NASAL ANTI-INFLAMMATORY STEROIDS |
GCN | 40708 |
HICL Sequence Number | 006545 |
HICL Sequence Number Description | BUDESONIDE |
Brand/Generic | Generic |
Proprietary Name | 4X Medicated Severe 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 | Rite Aid |
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 11822-0615-09 (11822061509)
NDC Package Code | 11822-0615-9 |
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Billing NDC | 11822061509 |
Package | 1 TUBE in 1 CARTON (11822-0615-9) / 7 g in 1 TUBE |
Marketing Start Date | 2020-05-06 |
NDC Exclude Flag | N |
Pricing Information | N/A |