Package 68229-601-02

Brand: sunburnt plus

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68229-601-02
Digits Only 6822960102
Product NDC 68229-601
Product ID 68229-601_12128c75-015e-8a72-e063-6394a90ae00a
Description

1 TUBE in 1 CARTON (68229-601-02) / 118 mL in 1 TUBE (68229-601-01)

Marketing

Marketing Status
Marketed Since 2024-02-23
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": "12128c75-015e-8a72-e063-6394a90ae00a", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010077"], "spl_set_id": ["12128c75-015d-8a72-e063-6394a90ae00a"], "manufacturer_name": ["Quest Products, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68229-601-02)  / 118 mL in 1 TUBE (68229-601-01)", "package_ndc": "68229-601-02", "marketing_start_date": "20240223"}], "brand_name": "SunBurnt PLUS", "product_id": "68229-601_12128c75-015e-8a72-e063-6394a90ae00a", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "68229-601", "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_start_date": "20240223", "listing_expiration_date": "20261231"}