Package 36800-894-01

Brand: topcare maximum strength pain relieving analgesic

Generic: menthol, unspecified form
NDC Package

Package Facts

Identity

Package NDC 36800-894-01
Digits Only 3680089401
Product NDC 36800-894
Product ID 36800-894_139ed16f-1958-417e-bf0e-4fe6f6f4ffaa
Description

1 BOTTLE, WITH APPLICATOR in 1 CARTON (36800-894-01) / 74 mL in 1 BOTTLE, WITH APPLICATOR

Marketing

Marketing Status
Marketed Since 2020-03-25
Brand topcare maximum strength pain relieving analgesic
Generic menthol, unspecified form
Sample Package No

Linked Drug Pages (1)

TopCare Maximum Strength Pain Relieving Analgesic ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "139ed16f-1958-417e-bf0e-4fe6f6f4ffaa", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["866084"], "spl_set_id": ["dc80d2f9-e3eb-4feb-bad5-7d6ab107f9ab"], "manufacturer_name": ["Topco Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, WITH APPLICATOR in 1 CARTON (36800-894-01)  / 74 mL in 1 BOTTLE, WITH APPLICATOR", "package_ndc": "36800-894-01", "marketing_start_date": "20200325"}], "brand_name": "TopCare Maximum Strength Pain Relieving Analgesic", "product_id": "36800-894_139ed16f-1958-417e-bf0e-4fe6f6f4ffaa", "dosage_form": "LIQUID", "product_ndc": "36800-894", "generic_name": "MENTHOL, UNSPECIFIED FORM", "labeler_name": "Topco Associates LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TopCare 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": "20200325", "listing_expiration_date": "20261231"}