Class II · Moderate risk
Hydroquinone USP
Finished product specification did not meet USP specifications.
National Drug Code
Is NDC 69367-0174-01 recalled?
Hydroquinone · 1 TUBE in 1 CARTON (69367-174-01) / 28.35 g in 1 TUBE
Yes — this exact package was recalled
2 FDA recalls name the code 69367-0174-01 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.
- Active ingredient
- Hydroquinone
- Strength
- HYDROQUINONE 40 mg/g
- Form
- Cream · Topical
- Labeler
- Westminster Pharmaceuticals, LLC
- Type
- Human Prescription Drug
- Product code
- 69367-0174
Recalls naming this package
Class III · Low risk
Hydroquinone
Subpotency: one product for active ingredient assay and another one for preservative assay
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
- 69367-0119 See recall 2
- 69367-0120 See recall 2
- 69367-0121 See recall 2
- 69367-0155 See recall 1
- 69367-0156 See recall 1
- 69367-0157 See recall 1
Free recall alerts
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