Package 44224-1040-1

Brand: after bite x tech

Generic: sodium bicarbonate
NDC Package

Package Facts

Identity

Package NDC 44224-1040-1
Digits Only 4422410401
Product NDC 44224-1040
Description

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

Marketing

Marketing Status
Marketed Since 2024-11-15
Brand after bite x tech
Generic sodium bicarbonate
Sample Package No

Linked Drug Pages (1)

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"}