Foamgle Foam Super Mint
- Product NDC
- 50555-220
- 11-digit product format
- 505550220
- Labeler code
- 50555
- Product ID
- 50555-220_4c006ee3-bf6a-e65c-e063-6294a90a4b96
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Allantoin
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- KMPHARMACEUTICAL CO.,LTD
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-02-01
- Substance
- ALLANTOIN
- Active strength
- .05 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Foamgle Foam Super Mint
- Listing expiration
- 2027-12-31
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 |
|---|
| 50555-220-01 | Foamgle Foam Super Mint | 150 mL in 1 BOTTLE | MOUTHWASH | 150 | | 1 |
| 50555-220-02 | Foamgle Foam Super Mint | 1 in 1 CARTON | MOUTHWASH | 1 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50555-220-01 | 50555022001 | 150 mL in 1 BOTTLE | 150 ml | | | | Historical |
| 50555-220-02 | 50555022002 | 1 BOTTLE in 1 CARTON (50555-220-02) / 150 mL in 1 BOTTLE (50555-220-01) | 1 bottle | 2026-02-01 | No | No | Current |