Act Whitening Anticavity Gentle Mint Mouthwash
Product Images NDC 41167-0983

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Act Whitening Anticavity Gentle Mint (NDC 41167-0983). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chattem, 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

Principal Display Panelactwhiteninganticavity Fluoride Mouthwashgentle Mint16.9 Fl Oz (500 mL) (Act Whitening Anticavity Fluoride Mouthwash Gentle 01)

Label of ACT Whitening Anticavity Fluoride Mouthwash in Gentle Mint flavor. It highlights zero alcohol and dye-free formula. The label states it is the #1 dentist recommended fluoride brand. Claims include whiter smile in 4 days, promoting oral health, strengthening and protecting teeth, and killing bad breath germs. The bottle size is 16.9 fl oz (500 mL).*

FDA Label Image

Principal Display Panelactwhiteninganticavity Fluoride Mouthwashgentle Mint16.9 Fl Oz (500 mL) (Act Whitening Anticavity Fluoride Mouthwash Gentle 02)

Drug Facts panel for ACT Whitening Anticavity Gentle Mint Mouthwash containing 0.02% sodium fluoride (0.009% w/v fluoride ion) as the active ingredient for anticavity use. Includes a warning to stop use if oral irritation or tooth sensitivity occurs and to keep out of reach of children. Directions specify use for adults and children 12 years and older, with supervision advised for children. Additional information lists inactive ingredients and advises not to use if the safety seal is broken or missing. The label also includes distributor details for Chattem, Inc., a Sanofi company.*

* 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.