CHINA-GEL WHITE (Camphor 3.00%, Menthol 5.00%), A TOPICAL PAIN RELIEVER, packaged in a) 2 oz(56.8g) Tube, 76305-301-13 ; b) 4 oz (113.5 g) jar, UPC 6 87806 20004 1, NDC 76305-301-02 ; c) 6 OZ (170 g) tube, UPC 6 87806 20006 5, NDC 76305-301-03; d) 8 oz (226.8 g) Jar, UPC 6 87806 20008 9, NDC 76305-301-04; e) 16 oz ( 453.6 g) Bottle w/ Pump, UPC 6 87806 20016 4, NDC 76305-301-05; f) 120 oz (3.78L) gallon, UPC 6 87806 20128 4, NDC 76305-301-06: Distributed by: CHINA-GEL LLC, Arlington Heights, IL 60005,
Drug Recall
Official source record
- Recall number
- D-0789-2021
- Event ID
- 87496
- Classification
- Class II
- Status
- Ongoing
- Recalling company
- China Gel Inc
- Reason for recall
- CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.
- Report date
- September 8, 2021
- Recall initiation date
- March 10, 2021
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Distributed Nationwide in the USA as well as Australia, Canada, France, Germany, Ireland, Norway, Turks & Caicos, Republic of Maldives, Russia, Singapore, Switzerland, United Kingdom
Drug product identifiers
- Manufacturer
- China-Gel, LLC
- Brand name
- CHINA-GEL
- Generic name
- MENTHOL AND CAMOHOR (SYNTHETIC)
- Substance names
- CAMPHOR (SYNTHETIC); MENTHOL
- Product NDC
- 76305-301
- Package NDCs
- 76305-301-02; 76305-301-03; 76305-301-04; 76305-301-05; 76305-301-06; 76305-301-07; 76305-301-13
- Route
- TOPICAL
Where this information comes from
View FDA enforcement record -- the specific openFDA drug enforcement record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for details, or FDA Enforcement Reports versus recall announcements for why that gap exists. New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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Frequently asked questions
What does a Class II mean?
FDA classifies this recall as Class II. See how to read an FDA recall record for what each classification level means.
Is this recall still active?
According to the FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this medication?
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Official guidance and record verification
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Compare the medication name, manufacturer, NDC, package information, and lot number on your medication with the official FDA record to see whether it matches.
Public Health Trace last retrieved this record on July 28, 2026.
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View the official FDA record · General drug recall guidance from FDA
Public Health Trace republishes official FDA drug recall information -- it is not affiliated with the FDA, does not verify or supplement what the source has published, and does not provide medical advice. Never start, stop, or change a medication based on this page. Always follow the guidance of your pharmacist or physician, and consult the official source links above for the most current information. Read the full medical disclaimer.