Package 72667-019-01

Brand: myderm bite relief

Generic: benzocaine
NDC Package

Package Facts

Identity

Package NDC 72667-019-01
Digits Only 7266701901
Product NDC 72667-019
Description

50 g in 1 TUBE (72667-019-01)

Marketing

Marketing Status
Marketed Since 2021-12-14
Brand myderm bite relief
Generic benzocaine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2d07a8c9-17a4-1727-e063-6394a90a801d", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "unii": ["U3RSY48JW5"], "rxcui": ["251295"], "spl_set_id": ["88615668-16b5-7840-e053-2a95a90a9208"], "pharm_class_cs": ["Allergens [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]"], "pharm_class_epc": ["Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["Inspec Solutions LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 TUBE (72667-019-01)", "package_ndc": "72667-019-01", "marketing_start_date": "20211214"}], "brand_name": "MyDerm Bite Relief", "product_id": "72667-019_2d07a8c9-17a4-1727-e063-6394a90a801d", "dosage_form": "OINTMENT", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "72667-019", "generic_name": "Benzocaine", "labeler_name": "Inspec Solutions LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MyDerm Bite Relief", "active_ingredients": [{"name": "BENZOCAINE", "strength": "5 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20211214", "listing_expiration_date": "20261231"}