Package 41250-350-01
Brand: meijer maximum strength pain relieving analgesic
Generic: menthol, unspecified formPackage 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
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"}