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 |
|---|---|---|---|---|---|---|
| Softlips Peppermint Swirl | DIMETHICONE | The Mentholatum Company | 4dbea50e-d82d-c702-e063-6394a90ac6e4 | 2026-03-24 | Warnings | M016 |
| Softlips Vanilla | DIMETHICONE | The Mentholatum Company | 56551008-a4e0-406f-8403-980d2e6b75a0 | 2026-03-24 | Warnings | M016 |
| Selan Plus Zinc Oxide | SELAN PLUS ZINC OXIDE | Trividia Manufacturing Solutions, Inc | 07396c61-1dfd-4be7-bddf-0eb570a18463 | 2026-03-24 | Warnings | M016 |
| D-Cerin | MOISTURIZER | Dynarex Corporation | 7ea47a7e-12af-9290-e053-2a91aa0a065f | 2026-03-24 | Warnings | M016 |
| MG217 Eczema Body | COLLOIDAL OATMEAL | Wisconsin Pharmacal Company | 5f0cfd0c-ae87-f411-e053-2a91aa0ac251 | 2026-03-20 | Warnings | M016 |
| Advanced Formula Scar Defense Cream | ALLANTOIN | Yantai Aien Biotechnology Co., Ltd. | 4d5c70f9-da41-b535-e063-6294a90a73f2 | 2026-03-19 | Warnings | M016 |
| TriplePaste Adult Care Rash Treatment | ZINC OXIDE | Advantice Health, LLC | 2cf0575c-8d3d-1f16-e063-6294a90a629d | 2026-03-19 | Warnings | M016 |
| multipurpose | ZINC OXIDE SKIN PROTECTANT | Advantice Health, LLC | 291563cc-7491-ce41-e063-6394a90ac6c1 | 2026-03-19 | Warnings | M016 |
| Triple Diaper Rash | ZINC OXIDE | Advantice Health, LLC | d457c58d-8239-41c4-999e-d0ba237e3945 | 2026-03-19 | Warnings | M016 |
| First Aid Beauty FAB Ultra Repair Intense Hydration Skin Protectant Cranberry Pomegranate | COLLOIDAL OATMEAL | The Procter & Gamble Manufacturing Company | f4464fb2-ba25-16f2-e053-2a95a90a0406 | 2026-03-19 | Warnings | M016 |
| First Aid Beauty FAB Ultra Repair Skin Protectant Vanilla Cookie | COLLOIDAL OATMEAL | The Procter & Gamble Manufacturing Company | fea4e5c7-780c-c7f4-e053-6294a90abb39 | 2026-03-19 | Warnings | M016 |
| Nicotine Patches | NICOTINE PATCHES | Zhejiang FTA Shengzuozhi Biotechnology Co., LTD | 4d46110b-5aa7-5261-e063-6394a90a423a | 2026-03-18 | Warnings | M016 |
| Advanced Bed Sore Wound Healing | ALLANTOIN | Yantai Aien Biotechnology Co., Ltd. | 4d589c18-e597-355a-e063-6394a90a4243 | 2026-03-18 | Warnings | M016 |
| MediChoice Barrier | DIMETHICONE | O&M HALYARD, INC. | 115c2a2f-d68a-316a-e063-6394a90a2716 | 2026-03-17 | Warnings | M016 |
| Nicotine Patches | NICOTINE PATCHES | Zhejiang FTA Shengzuozhi Biotechnology Co., LTD | 4d4427b0-25c3-ddf6-e063-6394a90a6153 | 2026-03-17 | Warnings | M016 |
| Colloidal Oatmeal | COLLOIDAL OATMEAL | Walmart Inc. | 4a93f77d-41dc-3bab-e063-6394a90a804b | 2026-03-16 | Warnings, Adverse reactions | M016 |
| Vaseline | HEALING JELLY | Conopco Inc. d/b/a Unilever | bd4418b7-c6aa-5e71-e053-2995a90a4cc4 | 2026-03-16 | Warnings | M016 |
| Vaseline Intensive Care Deep Moisture | PETROLEUM | Conopco Inc. d/b/a Unilever | 65cec560-25c7-4076-a33d-a3dd534ff85b | 2026-03-16 | Warnings | M016 |
| Daily Moisturizing | DAILY MOISTRUIZING | Walgreen Co. | 27452cc7-1ec6-4571-bcd0-0a7103735ee5 | 2026-03-13 | Warnings, Adverse reactions | M016 |
| Tender Moments Delicate Baby Diaper Rash Balm | DIMETHICONE,ZINC OXIDE | Distribuidora Comercial Jafra, S.A. de C.V. | f09ba452-e1a6-4f45-901f-bb63d4f8e884 | 2026-03-13 | 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 |