Orajel Kids Superman
- Product NDC
- 10237-732
- 11-digit product format
- 102370732
- Labeler code
- 10237
- Product ID
- 10237-732_2b47af33-32d5-7c06-e063-6394a90a2f33
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Anticavity Toothpaste
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Church & Dwight Co., Inc.
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-01-07
- Substance
- SODIUM FLUORIDE
- Active strength
- 1.5 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Orajel Kids Superman
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 1.5 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 416783 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10237-732-42 | Orajel Kids Superman | 119 g in 1 TUBE | GEL, DENTIFRICE | 119 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10237-732 | ORAJEL KIDS SUPERMAN (ANTICAVITY TOOTHPASTE) GEL, DENTIFRICE [CHURCH & DWIGHT CO., INC.] | 1 | Current NDC, 1 package rows | 20250112_2b47af33-32d4-7c06-e063-6394a90a2f33.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 10237-732-42 | 10237073242 | 119 g in 1 TUBE (10237-732-42) | 119 g | 2025-01-07 | No | No | Current |