CLASS II ONGOING Drug recall · Reported 5 Jun 2024 · FDA Enforcement Report

Natural Pain Relieving Cream, Golden Tiger, (Camphor recalled

ARG Laboratories is recalling Natural Pain Relieving Cream, Golden Tiger, (Camphor 3%, Menthol 3%)Enriched with, distributed nationwide in the US. The recall was initiated on 17 Apr 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 17323C3, Exp 06/30/2025
Quantity recalled1,680

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0529-2024
FDA event ID
94354
Recalling firm
ARG Laboratories, Dallas, TX
Classification
Class II
Status
Ongoing
Recall initiated
17 Apr 2024
FDA classified
30 May 2024
Reported
5 Jun 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

17 Apr 2024Recall initiated by company
30 May 2024Classified by FDA+43 days
5 Jun 2024Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

NATURAL PAIN RELIEVING CREAM, GOLDEN TIGER, (Camphor 3%, Menthol 3%)Enriched with Capsaicin, Aloe Vera, Willow Bark & MSM, Roll-On NET WT 3 fl. oz. (88.7ml), Manufactured for Golden Tiger USA Albuquerque, NM, UPC 1 82294 00006 2

Where it was distributed

Distributed Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

Out of Specification for active ingredient. Violative grade of propylene glycol used during the manufacturing process.

Which lots are affected?

Lot 17323C3, Exp 06/30/2025

Where was it sold?

Distributed Nationwide in the USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

10 other products · FDA event 94354

This product is part of a recall event; the main page for the event is Pain Wizard, Natural Relief for Muscular & Arthritic Pain recalled.

More recalls from ARG Laboratories

All 11

Other Natural Pain Relieving recalls

All 4