Package 41250-350-01

Brand: meijer maximum strength pain relieving analgesic

Generic: menthol, unspecified form
NDC Package

Package Facts

Identity

Package NDC 41250-350-01
Digits Only 4125035001
Product NDC 41250-350
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (41250-350-01) / 74 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2019-02-24
Brand meijer maximum strength pain relieving analgesic
Generic menthol, unspecified form
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2c052527-8626-4799-8c2c-1ebaa310890c", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["866084"], "spl_set_id": ["bd6f04f9-a23b-45f6-bce2-1ef7203198e1"], "manufacturer_name": ["Meijer Distribution, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (41250-350-01)  / 74 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "41250-350-01", "marketing_start_date": "20190224"}], "brand_name": "Meijer Maximum Strength Pain Relieving Analgesic", "product_id": "41250-350_2c052527-8626-4799-8c2c-1ebaa310890c", "dosage_form": "LIQUID", "product_ndc": "41250-350", "generic_name": "menthol, unspecified form", "labeler_name": "Meijer Distribution, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Meijer Maximum Strength Pain Relieving", "brand_name_suffix": "Analgesic", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "160 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190224", "listing_expiration_date": "20261231"}