Package 47682-321-02

Brand: pain relief

Generic: analgesic menthol
NDC Package

Package Facts

Identity

Package NDC 47682-321-02
Digits Only 4768232102
Product NDC 47682-321
Description

.059 L in 1 BOTTLE, SPRAY (47682-321-02)

Marketing

Marketing Status
Marketed Since 2019-04-01
Brand pain relief
Generic analgesic menthol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3e4ee639-9aef-38c5-e063-6394a90a9ad3", "openfda": {"upc": ["0347682301774"], "unii": ["L7T10EIP3A"], "spl_set_id": ["8162d22d-04c0-de07-e053-2991aa0a9975"], "manufacturer_name": ["Unifirst First Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".059 L in 1 BOTTLE, SPRAY (47682-321-02)", "package_ndc": "47682-321-02", "marketing_start_date": "20190401"}], "brand_name": "Pain Relief", "product_id": "47682-321_3e4ee639-9aef-38c5-e063-6394a90a9ad3", "dosage_form": "SPRAY", "product_ndc": "47682-321", "generic_name": "Analgesic Menthol", "labeler_name": "Unifirst First Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relief", "active_ingredients": [{"name": "MENTHOL", "strength": "70 mg/L"}], "application_number": "M015", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190401", "listing_expiration_date": "20261231"}