Hydromet Solution
Product Images NDC 0472-1030

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydromet (NDC 0472-1030). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Actavis Pharma, 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.

Product Images & Figures Index

FDA Label Image

Image 1

Image 1
The text appears to be a chemical equation indicating the molecular formula and weight of a compound. The compound consists of C1gHp1NO3, C4HgOg, and 21/2H,0 molecules with a molecular weight of 494.49 units.*
FDA Label Image

Image 2

Image 2
FDA Label Image

Image 3

Image 3
Hydromet is an oral prescription medication that contains hydrocodone bitartrate USP and homatropine methylbromide USP. This medication is typically used by adults and adolescents that are 12 years old and above. The usual dosage recommendation is one teaspoonful (5mL) every four to six hours as needed. Children between the ages of 6 to 11 years old are recommended one-half teaspoonful (2.5mL) every four to six hours. There is a maximum limit of six teaspoonfuls (30mL) in 24 hours and not more than three teaspoonfuls (15mL) in 24 hours for adults and children respectively. This medication should be stored at a controlled room temperature of 15° to 30°C (59° to 86°F) and should be dispensed in a tight, light-resistant container. The labeling should be checked for the lot number and expiration date. Distributed by Actavis Pharma, Inc of Parsippany, NJ, USA.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.