Goodsense Oral Pain Relief
- Product NDC
- 50804-191
- 11-digit product format
- 508040191
- Labeler code
- 50804
- Product ID
- 50804-191_483a8e8b-e815-3834-e063-6294a90a3225
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzocaine
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Geiss, Destin and Dunn, Inc.
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2014-05-09
- Substance
- BENZOCAINE
- Active strength
- 20 g/100g
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Goodsense Oral Pain Relief
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZOCAINE | 20 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U3RSY48JW5 |
| Rxcui | 238910 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50804-191-10 | Goodsense Oral Pain Relief | 1 in 1 CARTON | GEL | 1 | | 10 |
| 50804-191-10 | Goodsense Oral Pain Relief | 14 g in 1 TUBE | GEL | 14 | | 10 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| BENZOCAINE | ACTIVE INGREDIENT | U3RSY48JW5 | GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] | 1 | |
| BENZOCAINE | ACTIVE MOIETY | U3RSY48JW5 | GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] | 1 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] | 1 | |
| MINT | INACTIVE INGREDIENT | FV98Z8GITP | GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] | 1 | |
| POLYETHYLENE GLYCOL 400 | INACTIVE INGREDIENT | B697894SGQ | GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] | 1 | |
| POLYETHYLENE GLYCOL 4000 | INACTIVE INGREDIENT | 4R4HFI6D95 | GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] | 1 | |
| SACCHARIN SODIUM | INACTIVE INGREDIENT | SB8ZUX40TY | GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] | 1 | |
| SORBITOL | INACTIVE INGREDIENT | 506T60A25R | GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50804-191 | GOODSENSE ORAL PAIN RELIEF (BENZOCAINE) GEL [GEISS, DESTIN AND DUNN, INC.] | 9 | Current NDC, Legacy NDC, 2 package rows | 20220526_eb461b70-d10f-4e11-8374-e43713f3504d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50804-191-10 | 50804019110 | 1 TUBE in 1 CARTON (50804-191-10) / 14 g in 1 TUBE | 1 tube | 2018-12-18 | 0000-00-00 | No | No | Current |