Package 52000-414-06

Brand: universal witch hazel

Generic: witch hazel
NDC Package

Package Facts

Identity

Package NDC 52000-414-06
Digits Only 5200041406
Product NDC 52000-414
Description

177 mL in 1 BOTTLE, PLASTIC (52000-414-06)

Marketing

Marketing Status
Marketed Since 2023-07-01
Brand universal witch hazel
Generic witch hazel
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "66486f72-a425-450d-9669-0fa18a4899ee", "openfda": {"unii": ["101I4J0U34"], "spl_set_id": ["7e0b56ef-fa41-4862-b387-5b58d81d67d4"], "manufacturer_name": ["Universal Distribution Center LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (52000-414-06)", "package_ndc": "52000-414-06", "marketing_start_date": "20230701"}], "brand_name": "Universal WITCH HAZEL", "product_id": "52000-414_66486f72-a425-450d-9669-0fa18a4899ee", "dosage_form": "SOLUTION", "product_ndc": "52000-414", "generic_name": "witch hazel", "labeler_name": "Universal Distribution Center LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Universal WITCH HAZEL", "active_ingredients": [{"name": "WITCH HAZEL", "strength": "3 g/100mL"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230701", "listing_expiration_date": "20261231"}