United States · FDA National Drug Code directory

Still Standing

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
66902-167_4c0f6b65-79d8-db14-e063-6394a90aaeb9
Product NDC
66902-167
Form
LIQUID
Composition / generic term
MENTHOL, UNSPECIFIED FORM
Labeler
Natural Essentials Inc.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20230228
Source listing expiry
20271231

Source-listed ingredients

  • MENTHOL, UNSPECIFIED FORM — 100 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 15 mL in 1 BOTTLE, SPRAY (66902-167-15) · 66902-167-15
  • 15 mL in 1 BOTTLE, SPRAY (66902-167-17) · 66902-167-17
  • 18 mL in 1 BOTTLE, SPRAY (66902-167-18) · 66902-167-18
  • 100 mL in 1 BOTTLE, SPRAY (66902-167-34) · 66902-167-34

Source and coverage

Open FDA National Drug Code directory

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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