Product Images Dicyclomine Hydrochloride

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Product Label Images

The following 8 images provide visual information about the product associated with Dicyclomine Hydrochloride NDC 51662-1559 by Hf Acquisition Co Llc, Dba Healthfirst, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

POUCH LABELING - 51662 1559 2 POUCH LABEL

POUCH LABELING - 51662 1559 2 POUCH LABEL

This is a description of a medication called ION, USP. It contains dicyclomine hydrochloride, with a concentration of 20mg per 2mL (10mg per mL), and is intended for intramuscular use only. The medication is sterile and comes in a package that has an expiration date of January 1, 2025. The usual dosage is not provided in this text. The medicine should be stored between 20°C and 25°C (68°F and 77°F) and protected from freezing. Details about the packaging and the manufacturer are included, but it is recommended to see the manufacturer's package insert for further instructions.*

SERIALIZED CASE LABELING - 51662 1559 3 SERIALIZED LABELING

SERIALIZED CASE LABELING - 51662 1559 3 SERIALIZED LABELING

Case Labeling - 5166201559 3 CASE LABEL

Case Labeling - 5166201559 3 CASE LABEL

This is a description of an injectable drug called Dicyclomine Hydrochloride, which is contained in a vial. The vial contains 20mg per 2mL (10mg per 1mL) and has a lot number of 1234564 with an expiration date of 2025-01-01. The drug is to be used only for intramuscular injections, is sterile and comes in a solution made with sterile water and sodium chloride. It should be stored at 20-25°C and protected from freezing. The manufacturer is HF Acquisition Co., LLC located in Mukilteo, with an NDC number of 63323-842-02.*

ADVERSE - ADVERSE

ADVERSE - ADVERSE

HS - HS

HS - HS

This is a product with code 102 available in a unit of sale which contains 20mg per 2mL. It is packaged in a carton of 5 and each single-dose packaging contains 10mg per mL. The strength of each dose is not clearly specified. The product has two NDC codes i.e. 6332384202 and 63523-842-21.*

LOGO - LOGO

LOGO - LOGO

STRUCTURE - STRUCTURE

STRUCTURE - STRUCTURE

VIAL LABELING - VIAL LABELING

VIAL LABELING - VIAL LABELING

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.