Package 71874-080-42

Brand: daycon antibacterial foaming hand so ap

Generic: chloroxylenol
NDC Package

Package Facts

Identity

Package NDC 71874-080-42
Digits Only 7187408042
Product NDC 71874-080
Description

1250 mL in 1 PACKAGE (71874-080-42)

Marketing

Marketing Status
Marketed Since 2011-02-28
Brand daycon antibacterial foaming hand so ap
Generic chloroxylenol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "29a6f565-5181-2a29-e063-6394a90a28e5", "openfda": {"unii": ["0F32U78V2Q"], "spl_set_id": ["a37897d2-edfb-42f2-9a55-436965986512"], "manufacturer_name": ["Daycon Products Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1250 mL in 1 PACKAGE (71874-080-42)", "package_ndc": "71874-080-42", "marketing_start_date": "20110228"}], "brand_name": "DAYCON Antibacterial Foaming Hand So ap", "product_id": "71874-080_29a6f565-5181-2a29-e063-6394a90a28e5", "dosage_form": "LIQUID", "product_ndc": "71874-080", "generic_name": "Chloroxylenol", "labeler_name": "Daycon Products Company, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DAYCON Antibacterial Foaming Hand So ap", "active_ingredients": [{"name": "CHLOROXYLENOL", "strength": ".3 mg/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110228", "listing_expiration_date": "20261231"}