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Data / Drug companies / Shenzhen Shandian Jingling Technology Co., Ltd.

Shenzhen Shandian Jingling Technology Co., Ltd.: 21 products in the FDA NDC directory, labeler code 83804

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

Shenzhen Shandian Jingling Technology Co., Ltd. (labeler code 83804) lists 21 products in the FDA National Drug Code Directory, covering 13 finished drugs by generic name. By type: 21 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on November 2, 2026.

The request: Watch Shenzhen Shandian Jingling Technology Co., Ltd. (FDA labeler code 83804): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
83804
Products in commercial distribution
21
Packages
21
Finished drugs by generic name
13
Prescription products
0
Over the counter products
21
Flagged as original packager
18 of 18 products that carry the flag
Started marketing in the last 12 months
12
Earliest marketing start
March 27, 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 drugs21100%

Products by type

TypeProductsShare
Over the counter drugs21100%

Drugs it lists

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

DrugProductsCompanies listing it
Nicotine437
Tea tree oil32
Undecylenic acid 25%27
Sodium chloride271
Bee venom21
Glycerin156
Minoxidil1113
Vitamin d3, vitamin k211
Lidocaine 4%145
Minoxidil 5%18
Numbing12
Zingiber officinale (ginger) root extract11
Dioscorea villosa tuber12

Dosage forms

Dosage formProductsShare
Patch838.1%
Liquid523.8%
Cream523.8%
Aerosol, foam14.8%
Capsule14.8%
Solution14.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
SEFUDUN QUIT SMOKING NICOTINE PATCHES (21mg)83804-021PatchOver the counter monograph drugsNovember 2, 2026
SEFUDUN QUIT SMOKING NICOTINE PATCHES (14mg)83804-020PatchOver the counter monograph drugsNovember 2, 2026
SEFUDUN QUIT SMOKING NICOTINE PATCHES (7mg)83804-019PatchOver the counter monograph drugsNovember 2, 2026
Hatmanlabs Vitamin D3 K2 with Coconut Oil 120 Softgels83804-018CapsuleOver the counter monograph drugsApril 10, 2026
Worafy Gentle Eye Wash83804-017LiquidOver the counter monograph drugsMarch 23, 2026
Oimmal Gentle Eye Wash83804-016LiquidOver the counter monograph drugsFebruary 26, 2026
Marianp fungal nail patches83804-015PatchOver the counter monograph drugsFebruary 2, 2026
ELAIMEI Bee Venom Concentrated Cream83804-014CreamOver the counter monograph drugsJanuary 27, 2026
ELAIMEI Bee Venom Cream83804-013CreamOver the counter monograph drugsJanuary 27, 2026
WRFAATGO ANTIFUNGAL Pen Undecylenic Acid 25%83804-012LiquidOver the counter monograph drugsDecember 9, 2025
Elaimei fungal nail patches83804-011PatchOver the counter monograph drugsDecember 9, 2025
Lofuanna FUNGAL NAIL PATCHES83804-010PatchOver the counter monograph drugsNovember 18, 2025
Tktalker numbing83804-113CreamOver the counter monograph drugsAugust 29, 2025
Hair growth foam83804-008Aerosol, foamOver the counter monograph drugsAugust 22, 2025
Omzok antifungal pen83804-007LiquidOver the counter monograph drugsAugust 4, 2025
Sefudun fungal nail patches83804-006PatchOver the counter monograph drugsJuly 1, 2025
ELAIMEI Numbing Cream83804-005CreamOver the counter monograph drugsJune 16, 2025
YECUCE Wild Yam Cream83804-004CreamOver the counter monograph drugsJune 9, 2025
Hair Serum83804-003SolutionOver the counter monograph drugsMay 15, 2025
Sefudun nail fungus treatment83804-002LiquidOver the counter monograph drugsMay 9, 2025
Sefudun quit smoking nicotine patches83804-001PatchOver the counter monograph drugsMarch 27, 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.