flexdermal pain relieving roll-on
Generic: menthol
Labeler: solvaderm llcDrug Facts
Product Profile
Brand Name
flexdermal pain relieving roll-on
Generic Name
menthol
Labeler
solvaderm llc
Dosage Form
LIQUID
Routes
Active Ingredients
menthol 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
84197-867
Product ID
84197-867_2d76e34f-c583-4eae-e063-6294a90a5de5
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2025-01-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84197867
Hyphenated Format
84197-867
Supplemental Identifiers
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
flexdermal pain relieving roll-on (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 90 mL in 1 BOTTLE (84197-867-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}