Topical Anesthetic
- Product NDC
- 50227-2116
- 11-digit product format
- 502272116
- Labeler code
- 50227
- Product ID
- 50227-2116_69850139-6b9d-4bcd-b448-8a2fdb0bbfa5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Patterson Dental
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 1963-02-19
- Marketing end
- 0000-00-00
- Substance
- BENZOCAINE
- Active strength
- 220 mg/g
- Pharmacologic classes
- Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50227-2116-1 | Topical Anesthetic Banana | 34 g in 1 JAR | GEL, DENTIFRICE | 34 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50227-2116 | TOPICAL ANESTHETIC (BENZOCAINE) GEL, DENTIFRICE [PATTERSON DENTAL] | 1 | Legacy NDC, 1 package rows | 20100710_f4fdfcaf-aa95-45a8-ba91-7a8716f6f3d8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 50227-2116-1 | 50227211601 | 34 g in 1 JAR | 34 g | Historical |