United States · FDA National Drug Code directory

Dermasporin

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
87541-507_5738b40a-8261-9a9e-e063-6394a90a1f15
Product NDC
87541-507
Form
OINTMENT
Composition / generic term
Lanolin
Labeler
Marie's Original Formulas LLC
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20260710
Source listing expiry
20271231

Source-listed ingredients

  • LANOLIN — 3.96 g/14.2g

These values do not establish equivalence or a dose recommendation.

Packages

  • 14.2 g in 1 TUBE, WITH APPLICATOR (87541-507-04) · 87541-507-04

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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Dermasporin — United States | Molindra Medicines