Package 70000-0208-2

Brand: leader ultra strength muscle rub topical analgesic

Generic: camphor (synthetic), menthol, unspecified form, and methyl salicylate
NDC Package

Package Facts

Identity

Package NDC 70000-0208-2
Digits Only 7000002082
Product NDC 70000-0208
Product ID 70000-0208_e3f093f8-52f5-4130-a42b-8b3c8eb2a138
Description

1 TUBE in 1 CARTON (70000-0208-2) / 56.7 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2017-05-24
Brand leader ultra strength muscle rub topical analgesic
Generic camphor (synthetic), menthol, unspecified form, and methyl salicylate
Sample Package No

Linked Drug Pages (1)

Leader Ultra Strength Muscle Rub Topical Analgesic ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "e3f093f8-52f5-4130-a42b-8b3c8eb2a138", "openfda": {"unii": ["5TJD82A1ET", "L7T10EIP3A", "LAV5U5022Y"], "rxcui": ["283083"], "spl_set_id": ["9d99a900-60e0-454c-98e0-2c63eb910cf1"], "manufacturer_name": ["Cardinal Health, 110 dba LEADER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (70000-0208-1)  / 113 g in 1 TUBE", "package_ndc": "70000-0208-1", "marketing_start_date": "20170524"}, {"sample": false, "description": "1 TUBE in 1 CARTON (70000-0208-2)  / 56.7 g in 1 TUBE", "package_ndc": "70000-0208-2", "marketing_start_date": "20170524"}], "brand_name": "Leader Ultra Strength Muscle Rub Topical Analgesic", "product_id": "70000-0208_e3f093f8-52f5-4130-a42b-8b3c8eb2a138", "dosage_form": "CREAM", "product_ndc": "70000-0208", "generic_name": "Camphor (Synthetic), Menthol, Unspecified Form, and Methyl Salicylate", "labeler_name": "Cardinal Health, 110 dba LEADER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Leader Ultra Strength Muscle Rub", "brand_name_suffix": "Topical Analgesic", "active_ingredients": [{"name": "CAMPHOR (SYNTHETIC)", "strength": "40 mg/g"}, {"name": "MENTHOL, UNSPECIFIED FORM", "strength": "100 mg/g"}, {"name": "METHYL SALICYLATE", "strength": "300 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170524", "listing_expiration_date": "20261231"}