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
0316-0234_483436b1-9031-4992-e063-6394a90ad0c5
Product NDC
0316-0234
Form
LOTION
Composition / generic term
Pramoxine Hydrochloride, Menthol
Labeler
Crown Laboratories, Inc
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20240105
Source listing expiry
20271231

Source-listed ingredients

  • MENTHOL — .5 mg/1000mL
  • PRAMOXINE HYDROCHLORIDE — 10 mg/1000mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 355 mL in 1 BOTTLE, PUMP (0316-0234-12) · 0316-0234-12
  • 5 mL in 1 PACKET (0316-0234-24) · 0316-0234-24
  • 222 mL in 1 BOTTLE, PUMP (0316-0234-75) · 0316-0234-75

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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