Package 50289-3250-1

Brand: aer pre-moistened witch hazel pad

Generic: witch hazel
NDC Package

Package Facts

Identity

Package NDC 50289-3250-1
Digits Only 5028932501
Product NDC 50289-3250
Description

40 APPLICATOR in 1 JAR (50289-3250-1) / 2.8 mL in 1 APPLICATOR

Marketing

Marketing Status
Marketed Since 2018-06-28
Brand aer pre-moistened witch hazel pad
Generic witch hazel
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RECTAL", "TOPICAL"], "spl_id": "2baae3c5-a04e-c51e-e063-6394a90a81c3", "openfda": {"upc": ["0350289325012"], "unii": ["101I4J0U34"], "rxcui": ["844379", "1247719"], "spl_set_id": ["1cca622f-0a6b-4f35-9355-34c249ee705e"], "manufacturer_name": ["Birchwood Laboratories LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "40 APPLICATOR in 1 JAR (50289-3250-1)  / 2.8 mL in 1 APPLICATOR", "package_ndc": "50289-3250-1", "marketing_start_date": "20180628"}], "brand_name": "AER Pre-moistened Witch Hazel Pad", "product_id": "50289-3250_2baae3c5-a04e-c51e-e063-6394a90a81c3", "dosage_form": "SOLUTION", "product_ndc": "50289-3250", "generic_name": "Witch Hazel", "labeler_name": "Birchwood Laboratories LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AER", "brand_name_suffix": "Pre-moistened Witch Hazel Pad", "active_ingredients": [{"name": "WITCH HAZEL", "strength": "500 mg/mL"}], "application_number": "M015", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180628", "listing_expiration_date": "20261231"}