Hello Unicorn Sparkle
- Product NDC
- 35000-686
- 11-digit product format
- 350000686
- Labeler code
- 35000
- Product ID
- 35000-686_f02aba21-2ca9-4896-80b2-031b0430ecf4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM FLUORIDE
- Dosage form
- GEL, DENTIFRICE
- Route
- DENTAL
- Labeler
- Colgate-Palmolive Company
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-07-01
- Substance
- SODIUM FLUORIDE
- Active strength
- 1.1 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
- Hello Unicorn Sparkle
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM FLUORIDE | 1.1 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 416783 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 35000-686-10 | Hello Unicorn Sparkle | 1 in 1 CARTON | GEL, DENTIFRICE | 1 | | 3 |
| 35000-686-10 | Hello Unicorn Sparkle | 119 g in 1 TUBE | GEL, DENTIFRICE | 119 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 35000-686 | HELLO UNICORN SPARKLE (SODIUM FLUORIDE) GEL, DENTIFRICE [COLGATE-PALMOLIVE COMPANY] | 3 | Current NDC, 2 package rows | 20250515_5acfbd9b-278c-24dd-8041-5e2cdffbf710.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 |
|---|
| 35000-686-10 | 35000068610 | 1 TUBE in 1 CARTON (35000-686-10) / 119 g in 1 TUBE | 1 tube | 2023-07-01 | No | No | Current |