Package 72037-136-03
Brand: acuplus advanced therapy for pain and recovery
Generic: mentholPackage Facts
Identity
Package NDC
72037-136-03
Digits Only
7203713603
Product NDC
72037-136
Description
89 mL in 1 TUBE (72037-136-03)
Marketing
Marketing Status
Brand
acuplus advanced therapy for pain and recovery
Generic
menthol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0974c990-eb0f-73ff-e063-6294a90af414", "openfda": {"upc": ["0604286997698"], "unii": ["L7T10EIP3A"], "rxcui": ["1089766"], "spl_set_id": ["840cfd15-4ea1-49bf-8c4f-86c12461d860"], "manufacturer_name": ["INNOVATIONS FOR WELLNESS, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "89 mL in 1 TUBE (72037-136-03)", "package_ndc": "72037-136-03", "marketing_start_date": "20190501"}], "brand_name": "AcuPlus Advanced Therapy for Pain and Recovery", "product_id": "72037-136_0974c990-eb0f-73ff-e063-6294a90af414", "dosage_form": "SOLUTION", "product_ndc": "72037-136", "generic_name": "MENTHOL", "labeler_name": "INNOVATIONS FOR WELLNESS, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AcuPlus Advanced Therapy for Pain and Recovery", "active_ingredients": [{"name": "MENTHOL", "strength": "35 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190501", "listing_expiration_date": "20261231"}