After Bite X Tech
- Product NDC
- 44224-1040
- 11-digit product format
- 442241040
- Labeler code
- 44224
- Product ID
- 44224-1040_43d1291e-9392-6873-e063-6294a90ab2ac
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM BICARBONATE
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Adventure Ready Brands
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-01-01
- Substance
- SODIUM BICARBONATE
- Active strength
- 50 mg/1000mL
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Code | Status | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 44224-1040-0 | I | Inactivated by FDA | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded product | product | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… | |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 44224-1040-0 | I | Inactivated by FDA | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded product | product | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… | |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 44224-1040-0 | I | Inactivated by FDA | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded product | product | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… | |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 44224-1040-0 | I | Inactivated by FDA | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded product | product | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… | |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 44224-1040-0 | I | Inactivated by FDA | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded product | product | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… | |
| 2025-02-02 03:52 UTC · source 2025-01-31 | excluded package | package | 44224-1040-0 | U | Excluded because listing certification expired | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded product | product | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… | |
| 2025-01-20 13:05 UTC · source 2025-01-20 | excluded package | package | 44224-1040-0 | U | Excluded because listing certification expired | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded product | product | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… | |
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 44224-1040-0 | U | Excluded because listing certification expired | 0efc9e666f02… | f202fb6c5f17… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- After Bite X Tech
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM BICARBONATE | 50 mg/1000mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 8MDF5V39QO | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| e9e49ab4-3e1f-9fd4-e053-2a95a90a775a | Available on FDA.report |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 44224-1040-0 | 2025-11-17 | C162847 | 48780-1 | 2cef2736-a10c-d83d-e063-dadaa90ab31f | After Bite X Tech |
| 44224-1040-0 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-a10c-d83d-e063-dadaa90ab31f | After Bite X Tech |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 44224-1040-1 | After Bite X Tech | 1 in 1 BOX | LIQUID | 1 | 3 | |
| 44224-1040-1 | After Bite X Tech | 14 mL in 1 TUBE, WITH APPLICATOR | LIQUID | 14 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 44224-1040 | AFTER BITE X TECH (SODIUM BICARBONATE) LIQUID [ADVENTURE READY BRANDS] | 2 | Current NDC, Legacy NDC, 2 package rows | 20230120_e9e49ab4-3e1f-9fd4-e053-2a95a90a775a.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Boudreauxs | ZINC OXIDE | C.B. Fleet Company, Inc. | 59d90652-a471-4f77-a3d5-88aad9dc9e13 | 2025-10-30 | Warnings | M016 |
| CVS Cools Itch Fast | HYDROCORTISONE | CVS Pharmacy, Inc. | 8a4544df-bbba-47d2-ada0-352757abc91f | 2025-10-29 | Warnings | M016 |
| Winco Maximum Strength Hydrocortisone | HYDROCORTISONE | WINCO FOODS, LLC | b1812ea3-78cc-607a-e053-2a95a90a0a10 | 2025-10-29 | Warnings | M016 |
| Good Neighbor Pharmacy Skin Protectant | ZINC OXIDE | AMERISOURCE BERGEN | c28e63f1-34be-9206-e053-2995a90accf6 | 2025-10-29 | Warnings | M016 |
| Remedy Nutrashield | DIMETHICONE | Medline Industries, LP | ed8a08a7-594c-46e2-b70f-b75b2960141f | 2025-10-28 | Warnings | M016 |
| American Red Cross Anti-Itch | HYDROCORTISONE 1.0%(W/W) | MY IMPORTS USA LLC | 421da126-a1c4-54d7-e063-6394a90ac401 | 2025-10-27 | Warnings | M016 |
| GeriGard | ZINC OXIDE | Geri-Gentle Corporation | 05b67830-adc8-46b1-b0a0-a6cd2875e80c | 2025-10-27 | Warnings | M016 |
| Boudreauxs Butt Barrier | DIMETHICONE | C.B. Fleet Company, Inc. | 06a5af4d-40dd-42a4-8368-4d6a772d1b3a | 2025-10-27 | Warnings | M016 |
| WinCo Original Strength Anti-Itch | DIPHENHYDRAMINE HYDROCHLORIDE, AND ZINC ACETATE | WinCo Foods, LLC | ae74e163-ba1a-4d1e-aaeb-9976bd202674 | 2025-10-24 | Warnings | M016 |
| Maximum Strength Moisture Barrier | PETROLATUM AND ZINC OXIDE | Derma Sciences Canada Inc. | 41ee91c0-d196-cc0f-e063-6394a90a7b97 | 2025-10-24 | Warnings | M016 |
| Tenderphor | SKIN PROTECTANT | GERI-GENTLE CORPORATION | e6763da3-cbd1-7a86-e053-2995a90a26c1 | 2025-10-23 | Warnings | M016 |
| Boudreauxs | ZINC OXIDE | C.B. Fleet Company, Inc. | 262278f6-7e4c-44ee-b40d-39662a239d73 | 2025-10-23 | Warnings | M016 |
| American Red Cross Anti-Itch | HYDROCORTISONE 1.0%(W/W) | Zhejiang Guoyao Jingyue Aerosol Co., Ltd. | 41b8cb00-a04e-52f0-e063-6294a90aabf7 | 2025-10-22 | Warnings | M016 |
| WinCo Foods Hydrocortisone Cream Intensive Healing | HYDROCORTISONE | WINCO FOODS, LLC | ac4e0e24-9295-b83b-e053-2995a90a996f | 2025-10-22 | Warnings | M016 |
| JAFRA Fruteria Coco Fresco Lip Balm | DIMETHICONE | Distribuidora Comercial Jafra, S.A. de C.V. | 9895a320-8a74-4b27-9bf1-4b492f89888c | 2025-10-21 | Warnings | M016 |
| JAFRA Fruteria So Citrico | DIMETHICONE | Distribuidora Comercial Jafra, S.A. de C.V. | a68d6cda-2268-440a-9ca6-677c4e3ea0e7 | 2025-10-21 | Warnings | M016 |
| JAFRA Fruteria Very Verde Lip Balm | DIMETHICONE | Distribuidora Comercial Jafra, S.A. de C.V. | 4f0de70b-7ebe-4381-9b46-d5b334f426e0 | 2025-10-21 | Warnings | M016 |
| Gelmicin Hydrocortisone with Aloe | HYDROCORTISONE | United Exchange Corp. | bb64eca4-799d-4711-e053-2995a90af403 | 2025-10-21 | Warnings | M016 |
| Quadrydern | HYDROCORTISONE | Productos Zapotol Corp | a087ad4d-9a65-19c3-e053-2995a90ab341 | 2025-10-21 | Warnings | M016 |
| VENROCK | ROSEMARY OIL | Guangzhou Oupeng Cosmetics Co., Ltd | 4156b669-1817-6280-e063-6394a90aaf3a | 2025-10-17 | Warnings | M016 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 44224-1040-0 | 44224104000 | 1 TUBE, WITH APPLICATOR in 1 BOX (44224-1040-0) > 14 mL in 1 TUBE, WITH APPLICATOR | 2023-01-01 | 0000-00-00 | No | No | Current |
| 44224-1040-1 | 44224104001 | 1 TUBE, WITH APPLICATOR in 1 BOX (44224-1040-1) / 14 mL in 1 TUBE, WITH APPLICATOR | 2024-11-15 | No | No | Current |