Class II · Moderate risk
aulief (Organic Camphor 3.00% Organic Menthol 5.00%)
CGMP deviations: Product being recalled as it was made in the same facility where contamination with B. cepacia was found in other products.
National Drug Code
Is NDC 76305-0302-02 recalled?
Aulief Topical Pain Reliever · 198.5 g in 1 TUBE (76305-302-02)
Yes — this exact package was recalled
1 FDA recall names the code 76305-0302-02 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
1 of these recalls is still ongoing.
- Active ingredient
- Menthol and Camohor
- Strength
- CAMPHOR (NATURAL) 30 mg/g; MENTHOL 50 mg/g
- Form
- Cream · Topical
- Labeler
- China-Gel, LLC
- Type
- Human OTC Drug
- Product code
- 76305-0302
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 76305-0300 China-Gel Topical Pain Reliever 1
- 76305-0301 China-Gel Topical Pain Reliever 1
Free recall alerts
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