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Data / Drug companies / Lights Medical Manufacture Co., Ltd.

Lights Medical Manufacture Co., Ltd.: 19 products in the FDA NDC directory, labeler code 61333

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

Lights Medical Manufacture Co., Ltd. (labeler code 61333) lists 19 products in the FDA National Drug Code Directory, covering 4 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 August 7, 2026.

The request: Watch Lights Medical Manufacture Co., Ltd. (FDA labeler code 61333): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
61333
Products in commercial distribution
19
Packages
19
Finished drugs by generic name
4
Prescription products
0
Over the counter products
19
Flagged as original packager
19 of 19 products that carry the flag
Started marketing in the last 12 months
5
Earliest marketing start
February 22, 2014
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
Povidone-iodine858
Isopropyl alcohol5177
Benzocaine4110
Benzalkonium chloride2271

Dosage forms

Dosage formProductsShare
Solution1684.2%
Swab315.8%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
LIGHTS Antiseptic and Pain Relieving Prep Pad61333-222SolutionOver the counter monograph drugsAugust 7, 2026
Lights Povidone Iodine Swabsticks61333-221SolutionOver the counter monograph drugsJuly 22, 2026
Lights Alcohol Wipes61333-220SolutionOver the counter monograph drugsJune 24, 2026
Lights Medium Alcohol61333-219SwabOver the counter monograph drugsJune 24, 2026
Hug a BooBoo Medicated booboo Wipes61333-218SolutionOver the counter monograph drugsMarch 3, 2026
Lights Swabsticks61333-217SolutionOver the counter monograph drugsOctober 7, 2025
Lights Povidone Iodine Scrub61333-216SolutionOver the counter monograph drugsMay 20, 2025
LIGHTS Instant Sting Relief Pad61333-215SolutionOver the counter monograph drugsDecember 6, 2024
LIGHTS Insect Sting Relief Pad61333-213SolutionOver the counter monograph drugsJanuary 11, 2024
Lights Povindone Iodine Swabstick61333-212SwabOver the counter monograph drugsApril 3, 2023
LIGHTS Sting Relief Prep Pad61333-211SolutionOver the counter monograph drugsNovember 3, 2022
LIGHTS Swabstick61333-208SolutionOver the counter monograph drugsMarch 7, 2022
BZK Antiseptic61333-500SwabOver the counter monograph drugsJune 2, 2021
Lights Isopropyl Alcohol Prep Pads61333-206SolutionOver the counter monograph drugsAugust 1, 2019
Lights Povindone Iodine Scrub61333-205SolutionOver the counter monograph drugsJuly 18, 2019
Lights Povindone Iodine Swabstick61333-204SolutionOver the counter monograph drugsMarch 1, 2019
Lights Povidone Iodine Prep Pad61333-203SolutionOver the counter monograph drugsOctober 15, 2015
Lights Povidone Iodine Solution61333-202SolutionOver the counter monograph drugsMarch 22, 2014
Lights Povidone Iodine Solution61333-201SolutionOver the counter monograph drugsFebruary 22, 2014

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.