Package 48951-1394-2

Brand: arnica 20

Generic: arnica 20
NDC Package

Package Facts

Identity

Package NDC 48951-1394-2
Digits Only 4895113942
Product NDC 48951-1394
Description

30 g in 1 TUBE (48951-1394-2)

Marketing

Marketing Status
Marketed Since 2009-09-01
Brand arnica 20
Generic arnica 20
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2c90268b-b10a-2f14-e063-6294a90a54bc", "openfda": {"unii": ["O80TY208ZW"], "spl_set_id": ["2c90268b-b109-2f14-e063-6294a90a54bc"], "manufacturer_name": ["Uriel Pharmacy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 g in 1 TUBE (48951-1394-2)", "package_ndc": "48951-1394-2", "marketing_start_date": "20090901"}], "brand_name": "Arnica 20", "product_id": "48951-1394_2c90268b-b10a-2f14-e063-6294a90a54bc", "dosage_form": "OINTMENT", "product_ndc": "48951-1394", "generic_name": "Arnica 20", "labeler_name": "Uriel Pharmacy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arnica 20", "active_ingredients": [{"name": "ARNICA MONTANA", "strength": "1 [hp_X]/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}