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Prescription medicine · generic available

Permethrin

Drug class: Pyrethroid

The FDA’s “Established Pharmacologic Class”: the group of medicines that work in a similar way.

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

Quick answers

What is Permethrin used for?
The FDA-approved label (Elimite, Aurobindo Pharma Limited, January 24, 2024) says: “ELIMITE ® (permethrin) 5% Cream is indicated for the treatment of infestation with Sarcoptes scabiei (scabies).” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Does Permethrin have a boxed warning?
No. None of the 11 FDA labels we found for this medicine has a boxed warning.
Is there a shortage of Permethrin?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Permethrin been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Permethrin?
9 companies list prescription products of Permethrin in the FDA NDC Directory, including Bryant Ranch Prepack, Aurobindo Pharma Limited and Padagis Israel Pharmaceuticals Ltd.

What Permethrin is used for

Quoted from the “Indications and Usage” section of the FDA-approved label.

ELIMITE ® (permethrin) 5% Cream is indicated for the treatment of infestation with Sarcoptes scabiei (scabies).

— FDA label: Elimite, Aurobindo Pharma Limited, effective January 24, 2024. Read the full label on DailyMed →

The FDA has 11 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

Boxed warning

A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.

The label quoted above has no boxed warning.

0 of 11 FDA labels for this medicine have a boxed warning.

Forms and how it is given

Dosage formsCream
RouteTopical
Prescription products11 in the FDA NDC Directory
Brand namesElimite

What pharmacies pay (NADAC)

The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.

This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.

NADAC per unit for Permethrin, by strength and form
Strength and formGeneric or brandPharmacies pay
permethrin 5%
cream
Generic $0.2305 per gram
permethrin 50 mg/100 g
cream
Generic $0.2305 per gram

NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.

Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →

Companies that list this medicine

Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.

FDA approval history

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
  • ANDA: Abbreviated New Drug Application: how a generic version is approved.
Brand and biologic applications
ApplicationSponsorApprovedLater changes approved
NDA019855
ELIMITE
Aurobindo Pharma USAAugust 25, 1989 7, latest February 12, 2016
2016: Manufacturing (CMC) · 2001: Manufacturing (CMC) · 2001: Labeling

Generic approvals (3)

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.

Official identifiers

RxCUI (RxNorm)106387, 207485
SPL set ID of the quoted label443c0446-ccba-4f52-83ed-4c3163f35807
FDA labels (SPL)11
FDA applicationsNDA019855, 3 ANDA
Active ingredients (FDA)PERMETHRIN

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Elimite, Aurobindo Pharma Limited, effective January 24, 2024; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026

openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →

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