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 |
|---|---|---|---|---|---|---|
| Aveeno Baby Eczema Therapy Moisturizing | OATMEAL | Kenvue Brands LLC | 21d2c0a0-70c3-7fd3-e063-6394a90a46d4 | 2025-04-18 | Warnings | M016 |
| Secura Extra Protective | ZINC OXIDE | Smith & Nephew Medical Ltd | 499a1944-1682-4798-9058-3748a5eaa420 | 2025-04-17 | Warnings | M016 |
| Firming Care Gel | FIRMING CARE GEL | Guangzhou Jiaan Cosmetics Co.,Ltd. | 32cb8a71-81cd-cdbd-e063-6394a90ac07f | 2025-04-15 | Warnings | M016 |
| Baby Mantra Diaper Cream | ZINC OXIDE 10% | Renu Laboratories, LLC | 0427bbc9-f4c0-0eb6-e063-6294a90a7199 | 2025-04-14 | Warnings | M016 |
| Witch Hazel | WITCH HAZEL | TOP CARE (Topco Associates LLC) | 23b592f7-3af3-45ef-897a-fe33ab518b6d | 2025-04-14 | Warnings | M016 |
| Witch Hazel | WITCH HAZEL | Strategic Sourcing Services LLC | ef3408db-de98-4a43-9215-f80fed14815c | 2025-04-14 | Warnings | M016 |
| Petroleum Jelly | PETROLATUM | Walgreens | 69bdd508-7c33-42c5-9a08-e56cf3eaebf3 | 2025-04-11 | Warnings | M016 |
| 4% 10gTATTOO Numb Cream | 4% LIDOCAINE | Shengnan (Guangzhou) Cosmetics Co., LTD | 322daa32-a74e-1fee-e063-6294a90a37aa | 2025-04-07 | Warnings | M016 |
| Aluroderm Scar | ALLANTOIN | Asclemed USA, Inc. | 60656ca1-5218-4595-854e-19f1061def1e | 2025-04-01 | Warnings | M016 |
| Dr. Maxs Diaper | ZINC OXIDE | Dr. Maxs LLC | 31bfa962-5e3b-c5d2-e063-6294a90ac177 | 2025-04-01 | Warnings | M016 |
| Vaseline | BABY HEALING JELLY | Conopco Inc. d/b/a Unilever | bca3176f-86fe-5969-e053-2995a90a2419 | 2025-03-31 | Warnings | M016 |
| 4% TATTOO Numb Cream | 4% LIDOCAINE | Shengnan (Guangzhou) Cosmetics Co., LTD | 31646815-f591-c560-e063-6294a90ad11a | 2025-03-28 | Warnings | M016 |
| Face Saver Gel | SKIN PROTECTANT GEL | Neat Feat Products Limited | 31563dd7-9f58-80f6-e063-6294a90a5571 | 2025-03-27 | Warnings | M016 |
| Porphose | COLLOIDAL OATMEAL TOPICAL SPRAY | Porphose | 315951e0-899f-c968-e063-6294a90abe61 | 2025-03-27 | Warnings | M016 |
| Petroleum Jelly | WHITE PETROLATUM JELLY | WALGREENS | 1fc9eecd-fd25-827c-e063-6394a90a26a5 | 2025-03-26 | Warnings | M016 |
| Cocoa Butter Petroleum Jelly | WHITE PETROLATUM JELLY | WALGREENS | 1fcc9626-6058-e9b3-e063-6394a90ab525 | 2025-03-26 | Warnings | M016 |
| Nicotine Patches | NICOTINE PATCHES | Zhejiang FTA Shengzuozhi Biotechnology Co., LTD | 313b08e2-d764-96da-e063-6294a90ab705 | 2025-03-25 | Warnings | M016 |
| Eczema Cream | ECZEMA CREAM | Kyte Baby LLC | 30c943aa-d9dc-5c16-e063-6294a90a3c58 | 2025-03-20 | Warnings | M016 |
| Koala Kubs Diaper Rash Cream | DIAPER RASH CREAM | Melaleuca, Inc. | c6b3b0dd-22a8-16f7-e053-2a95a90a51ea | 2025-03-20 | Warnings | M016 |
| Gold Bond Eczema Relief Medicated Skin Protectant Cream | COLLOIDAL OATMEAL | Chattem, Inc. | 2b6b8342-878d-4588-8b24-6746d35d319d | 2025-03-19 | 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 |