Foamgle Foam Mouthwash Super Mint
- Product NDC
- 50555-210
- 11-digit product format
- 505550210
- Labeler code
- 50555
- Product ID
- 50555-210_352342bf-e2de-3a2c-e063-6294a90a200e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- KMPHARMACEUTICAL CO.,LTD
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-05-01
- Substance
- ALLANTOIN
- Active strength
- .05 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Foamgle Foam Mouthwash Super Mint
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALLANTOIN | .05 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 344S277G0Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50555-210-01 | Foamgle Foam Mouthwash Super Mint | 50 mL in 1 BOTTLE | LIQUID | 50 | | 1 |
| 50555-210-02 | Foamgle Foam Mouthwash Super Mint | 1 in 1 CARTON | LIQUID | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50555-210 | FOAMGLE FOAM MOUTHWASH SUPER MINT (ALLANTOIN) LIQUID [KMPHARMACEUTICAL CO.,LTD] | 1 | Current NDC, 2 package rows | 20250516_352342bf-e2dd-3a2c-e063-6294a90a200e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50555-210-01 | 50555021001 | 50 mL in 1 BOTTLE | 50 ml | | | | Historical |
| 50555-210-02 | 50555021002 | 1 BOTTLE in 1 CARTON (50555-210-02) / 50 mL in 1 BOTTLE (50555-210-01) | 1 bottle | 2025-05-01 | No | No | Historical |