Dicyclomine Hydrochloride Injection, Solution
Product Images NDC 70069-431

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Dicyclomine Hydrochloride (NDC 70069-431). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, Llc, 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

Image (A927b130 5b1b 462f Bb0c 2ea8763487ee 01)

Chemical structure diagram of DICYCLOMINE HYDROCHLORIDE representing its molecular composition including cyclohexyl groups, ester linkage, and ethyl-substituted amine with associated hydrochloride.*

FDA Label Image

Ampule-label (A927b130 5b1b 462f Bb0c 2ea8763487ee 02)

Label for Dicyclomine Hydrochloride Injection, USP 20 mg/2 mL (10 mg/mL) in a single-dose 2 mL ampule intended for intramuscular use. The label indicates the product is manufactured for Somerset Therapeutics, LLC, Somerset, NJ, and made in India. A barcode and NDC 70069-441-01 are also visible.*

FDA Label Image

Ampule-carton (A927b130 5b1b 462f Bb0c 2ea8763487ee 03)

Label for Dicyclomine Hydrochloride Injection, USP 20 mg/2 mL (10 mg/mL) intramuscular solution. The packaging contains 5 single-dose ampules of 2 mL each. Manufactured for Somerset Therapeutics, LLC, the label includes storage instructions and a barcode.*

FDA Label Image

Vial-label (A927b130 5b1b 462f Bb0c 2ea8763487ee 04)

Label for Dicyclomine Hydrochloride Injection, USP 20 mg/2 mL (10 mg/mL) single-dose vial. The label specifies the drug is for intramuscular use only and is manufactured for Somerset Therapeutics, LLC, Somerset, NJ. The product is made in India and includes an NDC 70069-431-01 and a barcode.*

FDA Label Image

Vial Carton (A927b130 5b1b 462f Bb0c 2ea8763487ee 05)

Label for Dicyclomine Hydrochloride Injection, USP 20 mg/2 mL (10 mg/mL) single-dose vials. The injection solution is for intramuscular use only and manufactured for Somerset Therapeutics, LLC. The label includes storage instructions and dosage strength with NDC 70069-431-05, for a package of 5 x 2 mL vials.*

* 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.