Package 0363-0641-18

Brand: hemorrhoidal cream

Generic: hemorrhoidal cream
NDC Package

Package Facts

Identity

Package NDC 0363-0641-18
Digits Only 0363064118
Product NDC 0363-0641
Description

1 TUBE in 1 PACKAGE (0363-0641-18) / 51 g in 1 TUBE (0363-0641-19)

Marketing

Marketing Status
Marketed Since 2018-03-25
Brand hemorrhoidal cream
Generic hemorrhoidal cream
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "485ead27-1d96-a01a-e063-6294a90a225a", "openfda": {"nui": ["N0000185370", "N0000175629", "N0000184306", "N0000185001", "M0000728", "M0009417"], "unii": ["PDC6A3C0OX", "4T6H12BN9U", "04JA59TNSJ", "88AYB867L5"], "rxcui": ["1293649"], "spl_set_id": ["4276ddad-2363-462a-bb97-574f946ec3f0"], "pharm_class_cs": ["Allergens [CS]", "Glycerol [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]", "Increased IgG Production [PE]"], "pharm_class_epc": ["Non-Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 PACKAGE (0363-0641-18)  / 51 g in 1 TUBE (0363-0641-19)", "package_ndc": "0363-0641-18", "marketing_start_date": "20180325"}], "brand_name": "Hemorrhoidal Cream", "product_id": "0363-0641_485ead27-1d96-a01a-e063-6294a90a225a", "dosage_form": "CREAM", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Allergens [CS]", "Cell-mediated Immunity [PE]", "Glycerol [CS]", "Increased Histamine Release [PE]", "Increased IgG Production [PE]", "Non-Standardized Chemical Allergen [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0363-0641", "generic_name": "Hemorrhoidal Cream", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Hemorrhoidal Cream", "active_ingredients": [{"name": "GLYCERIN", "strength": "144 mg/g"}, {"name": "PETROLATUM", "strength": "150 mg/g"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "2.5 mg/g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "M015", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180325", "listing_expiration_date": "20271231"}