Package 68229-600-01

Brand: sunburnt plus

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68229-600-01
Digits Only 6822960001
Product NDC 68229-600
Product ID 68229-600_4b23ad3d-3c31-6124-e063-6394a90a54f7
Description

1 TUBE in 1 CARTON (68229-600-01) / 118.294 mL in 1 TUBE (68229-600-02)

Marketing

Marketing Status
Discontinued 2026-07-31
Brand sunburnt plus
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

SunBurnt PLUS ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4b23ad3d-3c31-6124-e063-6394a90a54f7", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010077"], "spl_set_id": ["12de2559-05b0-4580-84c1-d3bd010b1c99"], "manufacturer_name": ["Quest Products, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68229-600-01)  / 118.294 mL in 1 TUBE (68229-600-02)", "package_ndc": "68229-600-01", "marketing_end_date": "20260731", "marketing_start_date": "20200701"}], "brand_name": "SunBurnt PLUS", "product_id": "68229-600_4b23ad3d-3c31-6124-e063-6394a90a54f7", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "68229-600", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "Quest Products, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SunBurnt PLUS", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "4 g/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20260731", "marketing_start_date": "20200701"}