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Data / Drug companies / Shanghai Chuangshi Medical Technology (Group) Co., Ltd.

Shanghai Chuangshi Medical Technology (Group) Co., Ltd.: 26 products in the FDA NDC directory, labeler code 73557

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

Shanghai Chuangshi Medical Technology (Group) Co., Ltd. (labeler code 73557) lists 26 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 26 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on October 8, 2026.

The request: Watch Shanghai Chuangshi Medical Technology (Group) Co., Ltd. (FDA labeler code 73557): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
73557
Products in commercial distribution
26
Packages
34
Finished drugs by generic name
6
Prescription products
0
Over the counter products
26
Flagged as original packager
24 of 24 products that carry the flag
Started marketing in the last 12 months
7
Earliest marketing start
December 22, 2022
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 drugs26100%

Products by type

TypeProductsShare
Over the counter drugs26100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Patch2076.9%
Gel415.4%
Cream13.8%
Lotion13.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
PAIN RELIEF Gel-Roll On73557-363GelOver the counter monograph drugsOctober 8, 2026
Foot Pain Relief Pads73557-190PatchOver the counter monograph drugsAugust 21, 2026
Lidocaine Numbing Cream73557-311CreamOver the counter monograph drugsAugust 20, 2026
Pain Relief Knee Gel-Patch73557-178PatchOver the counter monograph drugsAugust 3, 2026
Pain Relieving Gel-Patch73557-177PatchOver the counter monograph drugsJune 29, 2026
PAIN RELIEF Gel-Patch73557-176PatchOver the counter monograph drugsApril 20, 2026
Pain Relief73557-189PatchOver the counter monograph drugsNovember 10, 2025
Pain Relieving Gel-Patch73557-185PatchOver the counter monograph drugsOctober 15, 2025
Pain Relief73557-192PatchOver the counter monograph drugsSeptember 15, 2025
Pain Relief73557-187PatchOver the counter monograph drugsSeptember 15, 2025
Pain Relief73557-175PatchOver the counter monograph drugsSeptember 15, 2025
PAIN RELIEF Gel-Patch73557-174PatchOver the counter monograph drugsAugust 11, 2025
Pain Relieving Gel-Patch73557-160PatchOver the counter monograph drugsJune 11, 2025
OVERNIGHT RELIEF Gel-Patch73557-134PatchOver the counter monograph drugsJanuary 22, 2025
Pain Relieving Gel-Patch73557-159PatchOver the counter monograph drugsNovember 1, 2024
MENTHOL PAIN RELIEF Gel-Patch73557-131PatchOver the counter monograph drugsJanuary 9, 2024
Sunscreen-Lotion73557-575LotionOver the counter monograph drugsSeptember 13, 2023
Pain Relieving Gel-Patch73557-158PatchOver the counter monograph drugsJune 1, 2023
Pain Relieving Gel-Patch73557-180PatchOver the counter monograph drugsDecember 30, 2022
PAIN RELIEF Gel-Patch73557-172PatchOver the counter monograph drugsDecember 30, 2022
Pain Relieving Gel-Patch73557-157PatchOver the counter monograph drugsDecember 30, 2022
OVERNIGHT RELIEF Gel-Patch73557-133PatchOver the counter monograph drugsDecember 30, 2022
Elastic Relief Strip73557-130PatchOver the counter monograph drugsDecember 30, 2022
PAIN RELIEF Gel-Roll On73557-333GelOver the counter monograph drugsDecember 28, 2022
PAIN RELIEF Gel-Tube73557-323GelOver the counter monograph drugsDecember 28, 2022

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.