After Bite Advanced
- Product NDC
- 44224-1103
- 11-digit product format
- 442241103
- Labeler code
- 44224
- Product ID
- 44224-1103_4640051b-84fe-66c7-e063-6294a90a552e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Bicarbonate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Tender Corporation d/b/a Adventure Ready Brands
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-17
- Substance
- SODIUM BICARBONATE
- Active strength
- .7 g/14g
- Pharmacologic classes
- Alkalinizing Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- After Bite Advanced
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM BICARBONATE | .7 g/14g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8MDF5V39QO |
| Rxcui | 1547234 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 44224-1103-0 | After Bite Advanced | 1 g in 1 VIAL | LIQUID | 1 | | 4 |
| 44224-1103-2 | After Bite Advanced | 1 in 1 BOX | LIQUID | 1 | | 4 |
| 44224-1103-3 | After Bite Advanced | 14 g in 1 VIAL | LIQUID | 14 | | 4 |
| 44224-1103-3 | After Bite Advanced | 3 in 1 BOX | LIQUID | 3 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 44224-1103-0 | 44224110300 | 1 g in 1 VIAL | 1 g | | | | Historical |
| 44224-1103-2 | 44224110302 | 1 VIAL in 1 BOX (44224-1103-2) / 1 g in 1 VIAL (44224-1103-0) | 1 vial | 2025-06-17 | No | No | Historical |
| 44224-1103-3 | 44224110303 | 3 VIAL in 1 BOX (44224-1103-3) / 14 g in 1 VIAL | 3 vial | 2025-12-18 | No | No | Historical |