Dyna-hex Liquid
Product Images NDC 0116-1021

22 FDA label images from Xttrium Laboratories, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 22 technical images submitted to the FDA as part of the official labeling for Dyna-hex (NDC 0116-1021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xttrium 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

2dyn85 Df1

2dyn85 Df1
Drug Facts panel for DYNA-HEX 2 topical liquid with 2% chlorhexidine gluconate as the active antiseptic ingredient. The panel includes uses such as surgical hand scrub and healthcare personnel handwash to reduce microorganisms. It also lists warnings, including allergy alert for severe allergic reactions, and advises against use by those allergic to the product or its ingredients. Additional precautionary measures for use are included.*
FDA Label Image

2dyn85 Df2

2dyn85 Df2
A continuation panel of Drug Facts for DYNA-HEX 2, 2 g/100mL Chlorhexidine gluconate topical liquid by Xttrium Laboratories, Inc. It includes warnings about avoiding certain areas, seeking medical advice for irritation or allergic reactions, and keeping the product out of children's reach. Directions cover use in infants under 2 months, surgical hand scrub instructions, rinsing methods, and usage cautions to prevent irritation or chemical burns.*
FDA Label Image

2dyn85 Df3

2dyn85 Df3
Drug Facts panel continuation for DYNA-HEX 2 topical liquid with chlorhexidine gluconate 2 g/100mL. Includes healthcare personnel handwash instructions, storage temperature guidelines, inactive ingredients list, and a customer service contact number with hours. Also contains laundering and cleaning instructions advising against use of chlorine-based products.*
FDA Label Image

2dyn85 Front

2dyn85 Front
DYNA-HEX 2 Antimicrobial Hand Soap with Chlorhexidine Gluconate 2% Solution topical liquid. The label highlights its use as an antiseptic and states it contains 2% Chlorhexidine Gluconate. It is fragrance-free, FDA approved, and intended for external use only. The net contents are 8.5 fl oz (251 mL). The product is labeled by Xttrium Laboratories, Inc.*
FDA Label Image

Dyna Hex 16 Oz Nat Page 1

Dyna Hex 16 Oz Nat Page 1
Label for DYNA-HEX 2 Chlorhexidine Gluconate 2% Solution topical antiseptic liquid. Distributed by Xttrium Laboratories, Inc. The label states net contents as 16 fluid ounces (473 mL) and includes a barcode. A red banner states 'FOR EXTERNAL USE ONLY.'*
FDA Label Image

Dyna Hex 16 Oz Nat Page 2

Dyna Hex 16 Oz Nat Page 2
Drug Facts panel for DYNA-HEX 2 liquid topical antiseptic with 2% chlorhexidine gluconate. The panel lists active ingredient and purpose, uses including surgical hand scrub, healthcare personnel handwash, and skin cleansing, and warnings emphasizing external use only and allergy alerts with symptoms and instructions.*
FDA Label Image

Dyna Hex 16 Oz Nat Page 3

Dyna Hex 16 Oz Nat Page 3
Drug Facts panel for DYNA-HEX 2 (chlorhexidine gluconate 2 g/100mL topical liquid) provides warnings including allergy information, use precautions, and storage instructions. Directions detail surgical hand scrub, healthcare personnel handwash, and skin wound cleansing procedures. Other information includes storage temperature and inactive ingredients such as citric acid and cocamide DEA.*
FDA Label Image

Dyna Hex 16 Oz Nat Page 4

Dyna Hex 16 Oz Nat Page 4
This text panel from the DYNA-HEX 2 topical liquid drug label provides laundering and cleaning instructions, advising that chlorhexidine gluconate skin cleansers can stain when used with chlorine-releasing products and should be rinsed completely using non-chlorine detergents. It also includes a customer support contact number with hours of availability.*
FDA Label Image

Dyna Hex 16 Oz Page 1

Dyna Hex 16 Oz Page 1
Label for DYNA-HEX 2 Chlorhexidine Gluconate 2% Solution, a topical antiseptic liquid. The label states the active ingredient strength as 2% chlorhexidine gluconate, distributed by Xttrium Laboratories, Inc., Mount Prospect, IL. It includes a barcode, a warning for external use only, and net contents of 16 fluid ounces (473 mL).*
FDA Label Image

Dyna Hex 16 Oz Page 2

Dyna Hex 16 Oz Page 2
Drug Facts panel for DYNA-HEX 2% solution with the active ingredient chlorhexidine gluconate. It lists the product's purpose as an antiseptic and details uses including surgical hand scrub, healthcare personnel handwash, and skin wound cleansing. The panel also provides warnings about potential severe allergic reactions and advises external use only.*
FDA Label Image

Dyna Hex 16 Oz Page 3

Dyna Hex 16 Oz Page 3
A Drug Facts panel continuation for DYNA-HEX 2 containing chlorhexidine gluconate topical liquid. It includes sections on precautions (when not to use the product), detailed directions for surgical hand scrub, healthcare personnel handwash, and skin wound cleansing, as well as warnings about keeping out of eyes and contact with certain areas. Additional information covers storage instructions and lists inactive ingredients.*
FDA Label Image

Dyna Hex 16 Oz Page 4

Dyna Hex 16 Oz Page 4
A Drug Facts continuation panel providing contact information for questions or comments, including a phone number and available hours. It also includes laundering and cleaning instructions, specifically advising that chlorhexidine gluconate skin cleansers may cause stains if used with chlorine-releasing products like bleach and to rinse completely and use only non-chlorine detergents.*
FDA Label Image

Dyna Hex 1gal Page 1

Dyna Hex 1gal Page 1
Label for DYNA-HEX 2 Chlorhexidine Gluconate 2% Solution, a topical antiseptic liquid. The label shows the product name and strength, distributor information (Xttrium Laboratories, Inc., Mount Prospect, IL), a barcode, usage restriction for external use only, net contents of 128 fl oz (1 gallon), and a Drug Facts section highlighting chlorhexidine gluconate 2% as the active ingredient and antiseptic purpose.*
FDA Label Image

Dyna Hex 1gal Page 2

Dyna Hex 1gal Page 2
Drug Facts panel for DYNA-HEX 2 (Chlorhexidine gluconate 2g/100mL) topical liquid. The panel details uses including surgical hand scrub, healthcare personnel handwash, and skin wound cleansing. It includes warnings for allergy, usage precautions, and instructions to keep out of reach of children. Directions cover specific steps for surgical hand scrub, healthcare handwash, and skin wound cleansing application.*
FDA Label Image

Dyna Hex 1gal Page 3

Dyna Hex 1gal Page 3
Drug Facts panel continuation for DYNA-HEX 2 topical liquid (chlorhexidine gluconate 2 g/100 mL) includes storage instructions to keep at 20-25°C (68-77°F) and avoid heat above 40°C (104°F). Lists inactive ingredients: citric acid, cocamide DEA, hydroxyethylcellulose, isopropyl alcohol, lauramine oxide, purified water. Provides contact phone number and laundering/cleaning instructions advising against chlorine-releasing products.*
FDA Label Image

Dyna Hex 32 Oz Page 1

Dyna Hex 32 Oz Page 1
Label for DYNA-HEX 2 Chlorhexidine Gluconate 2% Solution antiseptic liquid. The label indicates a 2% chlorhexidine gluconate concentration, distributed by Xttrium Laboratories, Inc. Net contents are 32 fl oz (946 mL). The label warns FOR EXTERNAL USE ONLY and includes a barcode.*
FDA Label Image

Dyna Hex 32 Oz Page 2

Dyna Hex 32 Oz Page 2
Drug Facts panel for DYNA-HEX 2% Chlorhexidine gluconate topical liquid antiseptic. The panel details active ingredient, uses including surgical hand scrub and skin cleansing, warnings such as allergy alerts and usage precautions, and instructions for stopping use and keeping out of reach of children.*
FDA Label Image

Dyna Hex 32 Oz Page 3

Dyna Hex 32 Oz Page 3
Drug Facts panel continuing directions for use of DYNA-HEX 2 liquid topical solution containing chlorhexidine gluconate. It includes instructions for surgical hand scrub, healthcare personnel handwash, skin wound and general skin cleaning, storage information, listing of inactive ingredients, and a contact number for questions or comments. It also provides laundering and cleaning advice related to product use.*
FDA Label Image

Dyna Hex 8 Oz Page 1

Dyna Hex 8 Oz Page 1
Label of DYNA-HEX 2 topical liquid antiseptic showing Chlorhexidine Gluconate 2% solution with a net content of 8 fl oz (237 mL). Distributed by Xttrium Laboratories, Inc., Mount Prospect, IL. Includes a barcode and a warning for external use only.*
FDA Label Image

Dyna Hex 8 Oz Page 2

Dyna Hex 8 Oz Page 2
Drug Facts panel for DYNA-HEX 2, showing the active ingredient chlorhexidine gluconate 2% solution as an antiseptic. It lists uses including surgical hand scrub, healthcare personnel handwash, and skin wound cleansing. Warnings include external use only and allergy alert for potential severe allergic reactions such as wheezing or difficulty breathing.*
FDA Label Image

Dyna Hex 8 Oz Page 3

Dyna Hex 8 Oz Page 3
Drug Facts panel detailing warnings, precautions, and directions for use of DYNA-HEX 2 (Chlorhexidine gluconate 2 g/100mL) topical liquid. Includes allergy warnings, prohibited uses, advised precautions to avoid eye and ear injury, and instructions for surgical hand scrub and healthcare personnel handwash procedures with specific product use durations and rinsing steps.*
FDA Label Image

Dyna Hex 8 Oz Page 4

Dyna Hex 8 Oz Page 4
Drug Facts panel continuation for DYNA-HEX 2 topical liquid containing chlorhexidine gluconate, covering skin wound and general skin cleaning instructions, storage guidelines, inactive ingredients, contact information for questions, and laundering/cleaning instructions to avoid staining with chlorine bleach.*

* 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.