Package 84197-867-00

Brand: flexdermal pain relieving roll-on

Generic: menthol
NDC Package

Package Facts

Identity

Package NDC 84197-867-00
Digits Only 8419786700
Product NDC 84197-867
Description

90 mL in 1 BOTTLE (84197-867-00)

Marketing

Marketing Status
Marketed Since 2025-01-24
Brand flexdermal pain relieving roll-on
Generic menthol
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2d76e34f-c583-4eae-e063-6294a90a5de5", "openfda": {"upc": ["0659459675217"], "unii": ["L7T10EIP3A"], "spl_set_id": ["d4d8050e-0761-4491-8635-39c806701eb5"], "manufacturer_name": ["SOLVADERM LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 mL in 1 BOTTLE (84197-867-00)", "package_ndc": "84197-867-00", "marketing_start_date": "20250124"}], "brand_name": "FlexDermal Pain Relieving Roll-On", "product_id": "84197-867_2d76e34f-c583-4eae-e063-6294a90a5de5", "dosage_form": "LIQUID", "product_ndc": "84197-867", "generic_name": "MENTHOL", "labeler_name": "SOLVADERM LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FlexDermal Pain Relieving Roll-On", "active_ingredients": [{"name": "MENTHOL", "strength": "20 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250124", "listing_expiration_date": "20261231"}