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Data / Drug companies / Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.

Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.: 22 products in the FDA NDC directory, labeler code 83602

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. (labeler code 83602) lists 22 products in the FDA National Drug Code Directory, covering 4 finished drugs by generic name. By type: 22 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on August 21, 2026.

The request: Watch Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. (FDA labeler code 83602): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
83602
Products in commercial distribution
22
Packages
177
Finished drugs by generic name
4
Prescription products
0
Over the counter products
22
Flagged as original packager
19 of 19 products that carry the flag
Started marketing in the last 12 months
13
Earliest marketing start
August 8, 2023
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs22100%

Products by type

TypeProductsShare
Over the counter drugs22100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Lidocaine11216
Lidocaine and menthol917
Lidocaine 4%145
Menthol1263

Dosage forms

Dosage formProductsShare
Patch1672.7%
Gel522.7%
Cream14.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Knee pain relief roll-on83602-375GelOver the counter monograph drugsAugust 21, 2026
Heel pain relief roll-on83602-374GelOver the counter monograph drugsAugust 21, 2026
Big Toe Joint Pain Relief Patch83602-189PatchOver the counter monograph drugsAugust 21, 2026
Lidocaine Plantar Relief Roll-On83602-211GelOver the counter monograph drugsAugust 6, 2026
Lidocaine Numbing Cream83602-311CreamOver the counter monograph drugsJune 16, 2026
Knee Pain Relief Gel-Patch83602-178PatchOver the counter monograph drugsJune 12, 2026
Lidocaine Pain Relief Gel -Patch83602-231PatchOver the counter monograph drugsMay 15, 2026
Hip pain relief roll-on83602-773GelOver the counter monograph drugsApril 24, 2026
Heel pain relief roll-on83602-373GelOver the counter monograph drugsMarch 2, 2026
Lidocaine Pain Relief Gel -Patch83602-185PatchOver the counter monograph drugsFebruary 28, 2026
Lidocaine Pain Relief Gel-Patch83602-257PatchOver the counter monograph drugsFebruary 9, 2026
Lidocaine Pain Relief Gel-Patch83602-175PatchOver the counter monograph drugsJanuary 30, 2026
Foot Pain Relief Gel-Patch83602-174PatchOver the counter monograph drugsJanuary 24, 2026
Pain Relief Gel-Patch83602-172PatchOver the counter monograph drugsApril 10, 2025
LIDOCAINE PAIN RELIEF Gel-Patch83602-158PatchOver the counter monograph drugsApril 3, 2025
Lidocaine Pain Relief Gel-Patch83602-157PatchOver the counter monograph drugsMarch 24, 2025
Lidocaine Pain Relief Gel-Patch83602-157PatchOver the counter monograph drugsOctober 14, 2024
Menthol Overnight Pain Relief Gel-Patch83602-123PatchOver the counter monograph drugsFebruary 5, 2024
Pain Relief Gel-Patch83602-172PatchOver the counter monograph drugsNovember 28, 2023
Lidocaine Pain Relief Gel-Patch83602-157PatchOver the counter monograph drugsOctober 27, 2023
LIDOCAINE PAIN RELIEF Gel-Patch83602-158PatchOver the counter monograph drugsAugust 8, 2023
LIDOCAINE PAIN RELIEF Gel-Patch83602-158PatchOver the counter monograph drugsAugust 8, 2023

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.