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Data / Drug companies / GM Pharmaceuticals, Inc

GM Pharmaceuticals, Inc: 19 products in the FDA NDC directory, labeler code 58809

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

GM Pharmaceuticals, Inc (labeler code 58809) lists 19 products in the FDA National Drug Code Directory, covering 12 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 September 20, 2026.

The request: Watch GM Pharmaceuticals, Inc (FDA labeler code 58809): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
58809
Products in commercial distribution
19
Packages
23
Finished drugs by generic name
12
Prescription products
0
Over the counter products
19
Flagged as original packager
18 of 18 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
April 22, 2008
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 drugs1578.9%
Unapproved homeopathic products421.1%

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
Piperonyl butoxide, pyrethrum11
Dextromethorphan hbr, guaifenesin167
Pyrilamine maleate11
Chlophedianol hcl pyrilamine maleate11
Allergy relief14
Choline salicylate,guaifenesin11
Caffeine, choline salicylate11
Diaper rash cream12
Triprolidine hydrochloride13
Chlophedianol hcl, pyrilamine maleate11
Chlophedianol hcl, dexchlorpheniramine maleate11
Chlophedianol hydrochloride, pyrilamine maleate11

Dosage forms

Dosage formProductsShare
Liquid1052.6%
Solution315.8%
Solution/ drops210.5%
Gel15.3%
Tablet, chewable15.3%
Tablet15.3%
Cream15.3%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
TexaClear Mold Mix Allergy Relief58809-219LiquidUnapproved homeopathic productsSeptember 20, 2026
VanaCof 258809-190SolutionOver the counter monograph drugsDecember 14, 2023
VANACOF CP Allergy / Cough58809-189SolutionOver the counter monograph drugsDecember 6, 2023
VANACOF XP Cough / Chest Congestion58809-187SolutionOver the counter monograph drugsDecember 6, 2023
TexaClear Texas Allergy Relief plus Cedar Fever58809-215Tablet, chewableUnapproved homeopathic productsNovember 10, 2023
TexaClear Texas Allergy Relief plus Cedar Fever58809-214Solution/ dropsUnapproved homeopathic productsNovember 10, 2023
TexaClear All Season Allergy Relief58809-213Solution/ dropsUnapproved homeopathic productsNovember 10, 2023
TexaClear Pain and Chest Congestion Relief58809-218LiquidOver the counter monograph drugsOctober 25, 2023
TexaClear Severe Cough, Cold and Flu58809-217LiquidOver the counter monograph drugsOctober 25, 2023
Childrens PediaClear 858809-770LiquidOver the counter monograph drugsAugust 19, 2019
Childrens PediaClear PD58809-651LiquidOver the counter monograph drugsJuly 1, 2019
Vanalice58809-650GelOver the counter monograph drugsAugust 5, 2018
Texaclear pain reliever58809-389LiquidOver the counter monograph drugsDecember 14, 2017
TexaClear Kids Allergy58809-925LiquidOver the counter monograph drugsJune 15, 2016
Z-Bum58809-375CreamOver the counter monograph drugsDecember 1, 2015
TexaClear58809-186TabletOver the counter monograph drugsDecember 1, 2015
Texaclear Fast Acting Allergy Relief58809-360LiquidOver the counter monograph drugsOctober 21, 2014
Vanacof dm58809-555LiquidOver the counter monograph drugsJune 1, 2013
Vanacof58809-999LiquidOver the counter monograph drugsApril 22, 2008

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.