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Data / Drug companies / Guchutang Biotechnology (Longyan) Co., Ltd

Guchutang Biotechnology (Longyan) Co., Ltd: 19 products in the FDA NDC directory, labeler code 87083

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

Guchutang Biotechnology (Longyan) Co., Ltd (labeler code 87083) lists 19 products in the FDA National Drug Code Directory, covering 16 finished drugs by generic name. By type: 19 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on November 3, 2026.

The request: Watch Guchutang Biotechnology (Longyan) Co., Ltd (FDA labeler code 87083): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
87083
Products in commercial distribution
19
Packages
19
Finished drugs by generic name
16
Prescription products
0
Over the counter products
19
Flagged as original packager
10 of 10 products that carry the flag
Started marketing in the last 12 months
12
Earliest marketing start
October 22, 2025
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 drugs19100%

Products by type

TypeProductsShare
Over the counter drugs19100%

Drugs it lists

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

DrugProductsCompanies listing it
Diclofenac sodium2109
Pain relief23
Salicylic acid2330
Methyl salicylate, camphor and capsaicin11
Allantoin131
Multi-purpos treatment11
Intensive healing lotion11
Camphor mint11
Methyl saliclate capsaicin camphor11
Menthol methysalicylate11
Glacial acetic acid11
Relieve itching cream11
Foot odor11
Polyhexamethylene biguanide hydrochloride11
Wart remover112
Benzocaine1110

Dosage forms

Dosage formProductsShare
Cream947.4%
Liquid421.1%
Spray421.1%
Patch15.3%
Ointment15.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Zkbb arthritis pain relief87083-027CreamOver the counter monograph drugsNovember 3, 2026
Zkbb wart remover87083-026OintmentOver the counter monograph drugsNovember 2, 2026
Zkbb wart remover87083-025LiquidOver the counter monograph drugsNovember 2, 2026
Zkbb eczema87083-024CreamOver the counter monograph drugsNovember 2, 2026
Zkbb pain relief87083-022CreamOver the counter monograph drugsNovember 1, 2026
Toothache Relief87083-021SprayOver the counter monograph drugsOctober 31, 2026
Fungal nail treatment87083-020LiquidOver the counter monograph drugsOctober 29, 2026
Pain relief87083-013CreamOver the counter monograph drugsOctober 29, 2026
Zkbb arthritis pain relief87083-016CreamOver the counter monograph drugsOctober 5, 2026
Toothache87083-012SprayOver the counter monograph drugsJune 20, 2026
Sumifun Pain Relief Creams87083-011CreamOver the counter monograph drugsApril 12, 2026
Herbal Tendon Bone Relief87083-010PatchOver the counter monograph drugsDecember 15, 2025
Zourunan WART REMOVER87083-005LiquidOver the counter monograph drugsNovember 6, 2025
Zourunan PAIN RELIEF87083-007CreamOver the counter monograph drugsOctober 22, 2025
Zourunan PAIN RELIEF87083-006SprayOver the counter monograph drugsOctober 22, 2025
Zourunan FOOT ODOR PROBIOTIC87083-004SprayOver the counter monograph drugsOctober 22, 2025
Zourunan Relieve itching cream ANTIFUNGAL87083-003CreamOver the counter monograph drugsOctober 22, 2025
Zourunan Intensive healing lotion. for ECZEMA87083-002CreamOver the counter monograph drugsOctober 22, 2025
Zourunan MULTI-PURPOS TREATMENT87083-001LiquidOver the counter monograph drugsOctober 22, 2025

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.