Dometuss Liquid
Product Images NDC 65852-002

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Dometuss (NDC 65852-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dextrum Laboratories, Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Active (Dometuss Active Ingredients)

Active (Dometuss Active Ingredients)
Label for Dometuss liquid oral medication by Dextrum Laboratories, Inc. The label highlights the product as an antihistamine, cough suppressant, and nasal decongestant. It includes active ingredients chlorpheniramine maleate, dextromethorphan HBr, and phenylephrine HCl with their strengths in mg per 5 mL. The label features drug facts, usage information, a grape flavor indication, and lists inactive ingredients including sugar, alcohol, and dye. Bottle size noted as 4 fl oz (118 mL).*
FDA Label Image

Dometuss (Dometuss Central Display Panel)

Dometuss (Dometuss Central Display Panel)
Label for Dometuss, an oral liquid medication with Chlorpheniramine Maleate, Dextromethorphan HBr, and Phenylephrine HCL. The label highlights its use as an antihistamine, cough suppressant, and nasal decongestant. It shows a grape flavor and states the bottle contains 4 fl oz (118 mL). The labeler is Dextrum Laboratories, Inc. Drug facts and active ingredient strengths are printed in detail.*
FDA Label Image

Directions (Dometuss Directions Section)

Directions (Dometuss Directions Section)
Label for Dometuss liquid, an oral human OTC drug by Dextrum Laboratories, Inc. It contains Chlorpheniramine Maleate 2 mg/5 mL, Dextromethorphan HBr 10 mg/5 mL, and Phenylephrine HCL 5 mg/5 mL. The label features drug facts, dosage information, and a grape flavor indication. The package volume is 4 fl oz (118 mL).*
FDA Label Image

If Pregnant (Dometuss If Pregnant Section)

If Pregnant (Dometuss If Pregnant Section)
Dometuss liquid medication label indicating it as an antitussive, antihistamine, cough suppressant, and nasal decongestant. The label includes active ingredients Chlorpheniramine Maleate, Dextromethorphan HBr, and Phenylephrine HCL with strengths 2 mg/5 mL, 10 mg/5 mL, and 5 mg/5 mL respectively. It features a grape flavor indication, volume 4 fl oz (118 mL), and is labeled by Dextrum Laboratories, Inc.*
FDA Label Image

Inactive Ingredients (Dometuss Inactive Ingredients Section)

Inactive Ingredients (Dometuss Inactive Ingredients Section)
Label for Dometuss, an oral liquid cough suppressant, antihistamine, and nasal decongestant by Dextrum Laboratories, Inc. The label features dosage strength information and drug facts panels, indicates the flavor as grape, and lists inactive ingredients such as sugar, alcohol, and dye. The package volume is 4 fl oz (118 mL).*
FDA Label Image

Keep Out (Dometuss Keep Out Section)

Keep Out (Dometuss Keep Out Section)
Dometuss liquid oral solution label, containing Chlorpheniramine Maleate, Dextromethorphan HBr, and Phenylephrine HCL. The label highlights the product as an antihistamine, cough suppressant, and nasal decongestant. It shows a grape flavor indication and specifies a volume of 4 fl oz (118 mL). The label also includes drug facts panels, usage instructions, and manufacturer information for Dextrum Laboratories, Inc.*
FDA Label Image

Other Information (Dometuss Other Information Section)

Other Information (Dometuss Other Information Section)
Label for Dometuss liquid, an oral human OTC drug by Dextrum Laboratories, Inc. The label highlights its use as an antihistamine, cough suppressant, and nasal decongestant. It notes grape flavor and contains 4 fl oz (118 mL) per bottle. The label includes drug facts, active ingredient strengths, and directions for use.*
FDA Label Image

Purpose (Dometuss Purpose)

Purpose (Dometuss Purpose)
Label for Dometuss liquid by Dextrum Laboratories, Inc, an oral human OTC drug. The label highlights its use as an antihistamine, cough suppressant, and nasal decongestant. It shows active ingredients Chlorpheniramine Maleate, Dextromethorphan HBr, and Phenylephrine HCL with respective dosages, grape flavor indication, and volume 4 fl oz (118 mL). Drug facts and warnings are included on the label.*
FDA Label Image

Question (Dometuss Question Section)

Question (Dometuss Question Section)
Dometuss liquid oral medication label showing it contains Chlorpheniramine Maleate, Dextromethorphan HBr, and Phenylephrine HCL. The label includes usage as an antihistamine, cough suppressant, and nasal decongestant. It lists dosage strengths and includes a grape flavor indication. The labeler is Dextrum Laboratories, Inc, and the container volume is 4 fl oz (118 mL).*
FDA Label Image

Stop Use Section (Dometuss Stop Use Section)

Stop Use Section (Dometuss Stop Use Section)
Label for Dometuss oral liquid cough suppressant and nasal decongestant. Contains active ingredients Chlorpheniramine Maleate 2 mg/5 mL, Dextromethorphan HBr 10 mg/5 mL, and Phenylephrine HCL 5 mg/5 mL. The label shows dosage details, drug facts, sugar, alcohol, and dye information, grape flavor, and the Dextrum Laboratories, Inc. labeler name. The volume is 4 fl oz (118 mL).*
FDA Label Image

Tamper (Dometuss Tamper Evident Section)

Tamper (Dometuss Tamper Evident Section)
Label for Dometuss, an oral liquid containing Chlorpheniramine Maleate, Dextromethorphan HBr, and Phenylephrine HCL. It is an antihistamine, cough suppressant, and nasal decongestant product by Dextrum Laboratories, Inc. The label features drug facts, administration instructions, and a grape flavor indication for a 4 fl oz (118 mL) bottle.*
FDA Label Image

Warning (Dometuss Warnings Do Not Use)

Warning (Dometuss Warnings Do Not Use)
Label for Dometuss liquid oral solution, an antihistamine, cough suppressant, and nasal decongestant. Contains active ingredients Chlorpheniramine Maleate, Dextromethorphan HBr, and Phenylephrine HCL with strengths 2 mg/5 mL, 10 mg/5 mL, and 5 mg/5 mL respectively. The label shows grape flavor, sugar, alcohol, and dye content, with directions, warnings, and Drug Facts. Manufactured by Dextrum Laboratories, Inc.*
FDA Label Image

When Using Section (Dometuss When Using Section)

When Using Section (Dometuss When Using Section)
Label for Dometuss oral liquid, an antihistamine, cough suppressant, and nasal decongestant. The label shows it contains Chlorpheniramine Maleate, Dextromethorphan HBr, and Phenylephrine HCl with strengths of 2 mg, 10 mg, and 5 mg per 5 mL respectively. It is grape flavor, contains sugar, alcohol, and dye, and is manufactured by Dextrum Laboratories, Inc. The label includes drug facts and active ingredient information.*
FDA Label Image

Ask A Doctor (Dometuss Ask A Doctor)

Ask A Doctor (Dometuss Ask A Doctor)
The image shows the label for Dometuss liquid, an oral OTC drug by Dextrum Laboratories, Inc. It contains Chlorpheniramine Maleate 2 mg/5 mL, Dextromethorphan HBr 10 mg/5 mL, and Phenylephrine HCl 5 mg/5 mL. The label highlights its use as an antihistamine, cough suppressant, and nasal decongestant. The flavor is grape, and the bottle size is 4 fl oz (118 mL). Drug facts and ingredient details are also present.*
FDA Label Image

Indication And User (Dometuss Indication And User Section)

Indication And User (Dometuss Indication And User Section)
Dometuss liquid medication label showing proprietary name in blue and yellow. It is an antihistamine, cough suppressant, and nasal decongestant with active ingredients including Chlorpheniramine Maleate, Dextromethorphan HBr, and Phenylephrine HCl. The label notes 4 fl oz (118 mL) grape flavor and includes drug facts, uses, warnings, and inactive ingredients information. Manufactured by Dextrum Laboratories, Inc.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.