Package 30400-605-01

Brand: sunburn relief gel

Generic: lidocaine hcl
NDC Package

Package Facts

Identity

Package NDC 30400-605-01
Digits Only 3040060501
Product NDC 30400-605
Description

170 g in 1 BOTTLE, PUMP (30400-605-01)

Marketing

Marketing Status
Marketed Since 2025-02-19
Brand sunburn relief gel
Generic lidocaine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2e7c3924-521f-00bc-e063-6294a90a35da", "openfda": {"upc": ["0808829116144"], "unii": ["V13007Z41A"], "rxcui": ["1011849"], "spl_set_id": ["2e7c49de-5438-4858-e063-6294a90ad98c"], "manufacturer_name": ["Jell Pharmaceuticals Pvt. Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "170 g in 1 BOTTLE, PUMP (30400-605-01)", "package_ndc": "30400-605-01", "marketing_start_date": "20250219"}], "brand_name": "Sunburn Relief Gel", "product_id": "30400-605_2e7c3924-521f-00bc-e063-6294a90a35da", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "30400-605", "generic_name": "Lidocaine HCl", "labeler_name": "Jell Pharmaceuticals Pvt. Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sunburn Relief Gel", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "5 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250219", "listing_expiration_date": "20261231"}