Rycontuss Liquid
Product Images NDC 65852-021

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Rycontuss (NDC 65852-021). 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 Ingredient (Rycontus Active Ingredient)

Active Ingredient (Rycontus Active Ingredient)
Rycontuss Liquid 16 fl oz (473 mL) packaging label shows it as an oral liquid product with cherry flavor. It is labeled as an antitussive nasal decongestant and antihistamine. The label includes Drug Facts panels and the NDC 76171-001-16, with Dextrum Laboratories, Inc as the labeler.*
FDA Label Image

Ask A Doctor (Rycontus Ask A Doctor)

Ask A Doctor (Rycontus Ask A Doctor)
Rycontuss Liquid is an oral human OTC drug in 16 fl oz (473 mL) bottle size. It is a cherry-flavored antitussive nasal decongestant and antihistamine product. The label displays the brand name prominently with dosage information and Drug Facts panels on the front. The labeler is Dextrum Laboratories, Inc.*
FDA Label Image

Do Not Use (Rycontus Do Not Use Section)

Do Not Use (Rycontus Do Not Use Section)
Rycontuss Liquid cherry flavor antitussive nasal decongestant and antihistamine oral liquid medication. The label shows Drug Facts panels, product volume as 16 fl oz (473 mL), and the NDC number 76171-001-16. The label includes cherry graphics and is white and green with red and black text.*
FDA Label Image

Dosage (Rycontus Dosage And Administration)

Dosage (Rycontus Dosage And Administration)
Rycontuss Liquid, an oral liquid medication with cherry flavor, contains chlorpheniramine maleate 2 mg/5 mL, dextromethorphan hydrobromide 10 mg/5 mL, and phenylephrine hydrochloride 5 mg/5 mL. The label states it is an antitussive, nasal decongestant, and antihistamine. The bottle size is 16 fl oz (473 mL) and it is labeled by Dextrum Laboratories, Inc.*
FDA Label Image

Inactive (Rycontus Inactive Ingredient)

Inactive (Rycontus Inactive Ingredient)
Label of Rycontuss Liquid, a cherry-flavored oral liquid formulation. The product is an antitussive nasal decongestant and antihistamine. The label includes drug facts panels with active ingredients and usage information. The volume is 16 fl oz (473 mL). The manufacturer or labeler is not visible on this label.*
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Indication An User (Rycontus Indication And Usage)

Indication An User (Rycontus Indication And Usage)
Rycontuss Liquid Cherry Flavor is an oral liquid medication labeled as an antitussive, nasal decongestant, and antihistamine. The label indicates a 16 fl oz (473 mL) bottle. The product label includes drug facts panels and is manufactured by Dextrum Laboratories, Inc.*
FDA Label Image

Keep Out (Rycontus Keep Out Of Reach Of Children Section.)

Keep Out (Rycontus Keep Out Of Reach Of Children Section.)
Rycontuss Liquid cherry flavor is an oral liquid formulation containing chlorpheniramine maleate, dextromethorphan hydrobromide, and phenylephrine hydrochloride. The label specifies it as an antitussive, nasal decongestant, and antihistamine product. The packaging shows a 16 fl oz (473 mL) bottle and is labeled by Dextrum Laboratories, Inc.*
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Principal Panel (Rycontus Principal Panel)

Principal Panel (Rycontus Principal Panel)
Rycontuss Liquid cherry flavor antitussive nasal decongestant and antihistamine oral liquid, 16 fl oz (473 mL). The label includes drug facts panels and identifies the product as containing chlorpheniramine maleate, dextromethorphan hydrobromide, and phenylephrine hydrochloride. It shows dosage information and directions for use. Labeler is Dextrum Laboratories, Inc.*
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Purpose (Rycontus Purpose Section)

Purpose (Rycontus Purpose Section)
Rycontuss Liquid, a cherry flavor oral liquid containing chlorpheniramine maleate 2 mg/5 mL, dextromethorphan hydrobromide 10 mg/5 mL, and phenylephrine hydrochloride 5 mg/5 mL, is an antitussive, nasal decongestant, and antihistamine product by Dextrum Laboratories, Inc. The label shows a 16 fl oz (473 mL) bottle with Drug Facts and active ingredient information.*
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Pregnant (Rycontus Pregnancy Or Breast Feeding Section)

Pregnant (Rycontus Pregnancy Or Breast Feeding Section)
Rycontuss Liquid cherry flavor oral liquid, an antitussive nasal decongestant and antihistamine product. The label shows the brand name Rycontuss, the flavor as cherry, and the volume as 16 fl oz (473 mL). The label includes Drug Facts panels and lists the labeler as Dextrum Laboratories, Inc.*
FDA Label Image

Question (Rycontus Question)

Question (Rycontus Question)
Rycontuss Liquid is an oral over-the-counter human drug labeled as an antitussive, nasal decongestant, and antihistamine in cherry flavor. The product comes in a 16 fl oz (473 mL) bottle and contains chlorpheniramine maleate, dextromethorphan hydrobromide, and phenylephrine hydrochloride. It is labeled by Dextrum Laboratories, Inc.*
FDA Label Image

Stop Use (Rycontus Stop Use Section.)

Stop Use (Rycontus Stop Use Section.)
Rycontuss liquid pack label shows a cherry-flavored antitussive, nasal decongestant, and antihistamine product in a 16 fl oz (473 mL) bottle. The label includes drug facts panels, the active ingredients chlorpheniramine maleate, dextromethorphan hydrobromide, and phenylephrine hydrochloride, and the NDC 76171-001-16. It is labeled for oral liquid use and is marketed by Dextrum Laboratories, Inc.*
FDA Label Image

Warning (Rycontus Warnings Section)

Warning (Rycontus Warnings Section)
Rycontuss Liquid is an antitussive nasal decongestant and antihistamine oral liquid with cherry flavor, packaged in a 16 fl oz (473 mL) container. The label prominently features the product name, flavor, and usage, with drug facts detailing active ingredients and their purposes. The product is labeled with NDC 76171-001-16.*

* 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.