after bite x tech

Generic: sodium bicarbonate

Labeler: adventure ready brands
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name after bite x tech
Generic Name sodium bicarbonate
Labeler adventure ready brands
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

sodium bicarbonate 50 mg/1000mL

Manufacturer
Adventure Ready Brands

Identifiers & Regulatory

Product NDC 44224-1040
Product ID 44224-1040_43d1291e-9392-6873-e063-6294a90ab2ac
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M016
Listing Expiration 2026-12-31
Marketing Start 2023-01-01

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 442241040
Hyphenated Format 44224-1040

Supplemental Identifiers

UPC
0044224610409
UNII
8MDF5V39QO

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name after bite x tech (source: ndc)
Generic Name sodium bicarbonate (source: ndc)
Application Number M016 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1000mL
source: ndc
Packaging
  • 1 TUBE, WITH APPLICATOR in 1 BOX (44224-1040-1) / 14 mL in 1 TUBE, WITH APPLICATOR
source: ndc

Packages (1)

44224-1040-1 1 TUBE, WITH APPLICATOR in 1 BOX (44224-1040-1) / 14 mL in 1 TUBE, WITH APPLICATOR

Ingredients (1)

sodium bicarbonate (50 mg/1000mL)

Linked Drug Pages (1)

After Bite X Tech ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "43d1291e-9392-6873-e063-6294a90ab2ac", "openfda": {"upc": ["0044224610409"], "unii": ["8MDF5V39QO"], "spl_set_id": ["e9e49ab4-3e1f-9fd4-e053-2a95a90a775a"], "manufacturer_name": ["Adventure Ready Brands"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 BOX (44224-1040-1)  / 14 mL in 1 TUBE, WITH APPLICATOR", "package_ndc": "44224-1040-1", "marketing_start_date": "20241115"}], "brand_name": "After Bite X Tech", "product_id": "44224-1040_43d1291e-9392-6873-e063-6294a90ab2ac", "dosage_form": "LIQUID", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "44224-1040", "generic_name": "SODIUM BICARBONATE", "labeler_name": "Adventure Ready Brands", "product_type": "HUMAN OTC DRUG", "brand_name_base": "After Bite X Tech", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "50 mg/1000mL"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230101", "listing_expiration_date": "20261231"}