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 |
|---|---|---|---|---|---|---|
| Honest Eczema Balm | COLLOIDAL OATMEAL | The Honest Company, Inc. | 35b8bc5c-420e-4d31-9659-f36cabbd897a | 2024-05-14 | Warnings | M016 |
| Extra Strength Itch Stopping | ITCH STOPPING CREAM | Universal Distribution Centre LLC | b9a42aa3-1903-76f0-e053-2a95a90a51d1 | 2024-05-13 | Warnings | M016 |
| Calamine Clear | PRAMOXINE HYDROCHLORIDE AND ZINC ACETATE LOTION | Cardinal Health, 110 dba Leader | 7f733c0a-82b2-d3b0-e053-2991aa0a6b0f | 2024-05-13 | Warnings | M016 |
| Walgreens Maximum Diaper Rash | ZINC OXIDE | Walgreens Company | 5eb2152f-6fa2-4191-878a-207416e69818 | 2024-05-07 | Warnings | M016 |
| Cetaphil Eczema Rapid Relief Cream | COLLOIDAL OATMEAL | Galderma Laboratories, L.P. | 02a405fa-8ae9-41e9-b86f-ef5fb6e3844a | 2024-05-02 | Warnings | M016 |
| Chapstick | AVOBENZONE, OCTINOXATE, AND WHITE PETROLATUM | Haleon US Holdings LLC | 0e34fc74-772e-48fd-a353-58807ef412c1 | 2024-05-01 | Warnings | M016 |
| Diaper Rash Cream 40% ZINC | ZINC OXIDE | ASTONEA LABS PRIVATE LIMITED | 16da985a-6210-ec82-e063-6294a90a132d | 2024-04-24 | Warnings | M016 |
| Petrolatum Jelly | PETROLATUM | ASTONEA LABS PRIVATE LIMITED | 16dac8e5-aeb8-592d-e063-6394a90ae2b6 | 2024-04-24 | Warnings | M016 |
| Monistat Complete Care Chafing Relief | DIMETHICONE | Insight Pharmaceuticals LLC | 07d7c883-1fa3-4786-905c-a1fab649765e | 2024-04-19 | Warnings | M016 |
| zinc oxide 20% | ZINC OXIDE 20% | Bionpharma Inc | 1549500a-0941-0fba-e063-6394a90a564e | 2024-04-18 | Warnings | M016 |
| ARC Skin Protectant | ALLANTOIN | Anjon Biologics, Inc | f4ff79dd-cb38-4cca-9631-a2758a171873 | 2024-04-18 | Warnings | M016 |
| Zinctral | ZINC OXIDE | PureTek Corporation | de990834-00da-0c7a-e053-2995a90a7c37 | 2024-04-15 | Warnings | M016 |
| Chapstick Moisturizer Variety Pack | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, WHITE PETROLATUM | Haleon US Holdings LLC | bfb9a2d5-1ad2-45b8-a215-9d1370af5337 | 2024-04-12 | Warnings | M016 |
| ChapStick Classic Spearmint | PETROLATUM | Haleon US Holdings LLC | d39786e8-bcd8-479d-8990-142a21788a47 | 2024-04-12 | Warnings | M016 |
| Chapstick 12 Days of Christmas | WHITE PETROLATUM | Haleon US Holdings LLC | d6eb2ea6-27c7-40a6-a1f0-789ea2131de3 | 2024-04-11 | Warnings | M016 |
| Chapstick Active 2in1 Variety Pack | ZINC OXIDE | Haleon US Holdings LLC | d1998a9e-d61f-4b4c-91b0-5e66754bcc4a | 2024-04-11 | Warnings | M016 |
| Chapstick 12 Days of Christmas | WHITE PETROLATUM | Haleon US Holdings LLC | 040694f0-b5ba-4203-bde9-699fa9b1afef | 2024-04-11 | Warnings | M016 |
| Chapstick Holiday Classics Kit | WHITE PETROLATUM | Haleon US Holdings LLC | 6df216dc-c03d-463a-8029-5e54c1dc3d27 | 2024-04-11 | Warnings | M016 |
| Carmex Classic Lip Balm Medicated SPF15 Triple Force Formula | OCTINOXATE, OXYBENZONE, WHITE PETROLATUM | Carma Laboratories, Inc. | 3eb0f8ff-89e7-4410-8573-3349e4946548 | 2024-04-02 | Warnings | M016 |
| Pure Cornstarch Baby | CORN STARCH | Walgreen Company | d0e9bd13-b568-4f7e-b036-8d23e71ad8bf | 2024-03-25 | 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 |