Orajel
- Product NDC
- 10237-734
- 11-digit product format
- 102370734
- Labeler code
- 10237
- Product ID
- 10237-734_4b80947d-f38a-2f80-e063-6294a90abd55
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium fluoride
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Church & Dwight Co., Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-05
- Substance
- SODIUM FLUORIDE
- Active strength
- 1.5 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Orajel
- Brand name suffix
- Toy Story 5 Anticavity
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 1.5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10237-734-42 | OrajelToy Story 5 Anticavity | 119 g in 1 TUBE | GEL, DENTIFRICE | 119 | | 1 |
| 10237-734-58 | OrajelToy Story 5 Anticavity | 164 g in 1 TUBE | GEL, DENTIFRICE | 164 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 10237-734-42 | 10237073442 | 119 g in 1 TUBE (10237-734-42) | 119 g | 2026-01-05 | No | No | Current |
| 10237-734-44 | 10237073444 | 4 TUBE in 1 CARTON (10237-734-44) / 119 g in 1 TUBE | 4 tube | 2026-06-01 | 0 | | Current |
| 10237-734-58 | 10237073458 | 164 g in 1 TUBE (10237-734-58) | 164 g | 2026-01-05 | No | No | Current |