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 01623C1, Exp 01/31/2025
Quantity recalled3,000

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-0527-2024
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, Tube 4 oz (113.39 g), Mfr. for Golden Tiger USA Albuq, NM, UPC 1 82294 00002 4

Where it was distributed

Distributed Nationwide in the USA

Nationwide

Questions about this recall

Is Natural Pain Relieving Cream, Golden Tiger, (Camphor 3%, Menthol 3%)Enriched with recalled?

Yes. ARG Laboratories recalled Natural Pain Relieving Cream, Golden Tiger, (Camphor 3%, Menthol 3%)Enriched with on 17 Apr 2024. The recall is Class II and its status is Ongoing. Recall number D-0527-2024.

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 01623C1, Exp 01/31/2025

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

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