Package 13709-239-01

Brand: neilmed anti-itch

Generic: anti-itch spray
NDC Package

Package Facts

Identity

Package NDC 13709-239-01
Digits Only 1370923901
Product NDC 13709-239
Description

90 g in 1 CAN (13709-239-01)

Marketing

Marketing Status
Marketed Since 2020-11-11
Brand neilmed anti-itch
Generic anti-itch spray
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0eb0a47d-4c98-a632-e063-6394a90a29dd", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["WI4X0X7BPJ"], "spl_set_id": ["b3d34d9e-85d9-df4e-e053-2a95a90ac8d9"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["NeilMed Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 g in 1 CAN (13709-239-01)", "package_ndc": "13709-239-01", "marketing_start_date": "20201111"}], "brand_name": "NeilMed Anti-Itch", "product_id": "13709-239_0eb0a47d-4c98-a632-e063-6394a90a29dd", "dosage_form": "SPRAY", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "13709-239", "generic_name": "Anti-Itch Spray", "labeler_name": "NeilMed Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NeilMed Anti-Itch", "active_ingredients": [{"name": "HYDROCORTISONE", "strength": "1 g/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20201111", "listing_expiration_date": "20261231"}