Package 82442-088-07

Brand: up and up

Generic: benzalkonium chloride
NDC Package

Package Facts

Identity

Package NDC 82442-088-07
Digits Only 8244208807
Product NDC 82442-088
Product ID 82442-088_427bb3c4-9952-b4db-e063-6294a90ad158
Description

222 mL in 1 BOTTLE, PLASTIC (82442-088-07)

Marketing

Marketing Status
Marketed Since 2025-10-22
Brand up and up
Generic benzalkonium chloride
Sample Package No

Linked Drug Pages (1)

UP and UP ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "427bb3c4-9952-b4db-e063-6294a90ad158", "openfda": {"upc": ["0191907923223"], "unii": ["F5UM2KM3W7"], "rxcui": ["1046593"], "spl_set_id": ["39855595-cd79-a116-e063-6294a90a9638"], "manufacturer_name": ["TARGET CORPORATION INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "222 mL in 1 BOTTLE, PLASTIC (82442-088-07)", "package_ndc": "82442-088-07", "marketing_start_date": "20251022"}], "brand_name": "UP and UP", "product_id": "82442-088_427bb3c4-9952-b4db-e063-6294a90ad158", "dosage_form": "LIQUID", "product_ndc": "82442-088", "generic_name": "Benzalkonium Chloride", "labeler_name": "TARGET CORPORATION INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "UP and UP", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "130 mg/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251022", "listing_expiration_date": "20261231"}