Product Images Onelax

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Product Label Images

The following image provide visual information about the product associated with Onelax NDC 71399-0039 by Akron Pharma, 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.

label - one lax docsod

label - one lax docsod

This is a description of a drug called Docusate Sodium. It is a stool softener laxative used to relieve occasional constipation. The active ingredient in each 5 mL of the drug is 50 mg of Docusate Sodium. The drug generally produces a bowel movement within 12 to 72 hours. It is important to not use this drug for more than one week unless directed by a doctor. Before using this drug, it is advised to consult a doctor if you have stomach pain, nausea, vomiting, sudden change in bowel habits that persists for more than 2 weeks, or if you are currently taking mineral oil. Stop using the drug and consult a doctor if you experience rectal bleeding, fail to have a bowel movement after use, develop a skin rash, or experience throat irritation. Pregnant or breastfeeding individuals should consult a doctor before using this drug. It should be kept out of reach of children, and in case of accidental overdose, medical assistance or Poison Control Center should be contacted immediately. The drug should be shaken well before use and the dosing directions on the label should be followed. The recommended dose should not be exceeded. It is recommended to take the drug with a 6 to 8 oz glass of milk or fruit juice to prevent throat irritation. The maximum dose should be taken daily until the first bowel movement, after which the dosage should be reduced according to individual response. The drug is in liquid form and each teaspoonful (5 ml) contains 5 mg of sodium. It should be stored at room temperature, protected from excessive heat. The bottle opening should not be used if the foil is torn, broken, or missing. The drug contains inactive ingredients such as citric acid, red dye, vanilla flavor, glycerin, parabens, poloxamer 407, purified water, sodium benzoate, sodium citrate, sorbitol solution, and sucralose. For any questions or comments, a toll-free number is provided. The drug is manufactured by Akron Pharma, Inc. and further information can be found on their website.*

* 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.