United States · FDA National Drug Code directory

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A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
63936-8523_4f9a81e5-ae55-4fa6-e063-6294a90a218e
Product NDC
63936-8523
Form
LIQUID
Composition / generic term
MENTHOL
Labeler
TROY MANUFACTURING, INC
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20101013
Source listing expiry
20271231

Source-listed ingredients

  • MENTHOL — 80 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 88 mL in 1 BOTTLE, WITH APPLICATOR (63936-8523-1) · 63936-8523-1
  • 1 BOTTLE, WITH APPLICATOR in 1 BOX (63936-8523-2) / 88 mL in 1 BOTTLE, WITH APPLICATOR · 63936-8523-2

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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