Product Images Ranitidine Hydrochloride Oral Suspension Kit

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Product Label Images

The following 5 images provide visual information about the product associated with Ranitidine Hydrochloride Oral Suspension Kit NDC 70332-109 by California Pharmaceuticals, Llc, 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.

Oral Suspension Vehicle Label - Oral Suspension Vehicle Label

Oral Suspension Vehicle Label - Oral Suspension Vehicle Label

This is an oral suspension product from California Pharmaceuticals LLC with a pineapple/orange flavor. It does not contain sugar, dye, and paraben but mainly comprises purified water, glycerin, pineapple and orange flavor, potassium sorbate, xanthan gum, etc. The net contents of the product are 250mL (8.4 fl oz). However, the text does not provide any information about the purpose of the product.*

Ranitidine Hydrochloride Principle Display - Ranitidine Hydrochloride Principle Display

Ranitidine Hydrochloride Principle Display - Ranitidine Hydrochloride  Principle Display

This text provides information about a Ranitidine Hydrochloride Oral Suspension kit containing active and inactive materials to prepare a medication with specialized needs. The kit is repackaged and distributed by California Pharmaceuticals, LLC, and contains 25.0 mg/mL of Ranitidine Hydrochloride. The kit is to be used for prescription compounding only upon a physician's prescription by an appropriate licensed medical professional. The kit contains active ingredients such as ranitidine hydrochloride USP and inactive ingredients like purified water, glycerin, and potassium sorbate. Moreover, the description mentions that the Ranitidine Hydrochloride Oral Suspension should be stored at room temperature, and that the kit should not be used if the safety seal is broken.*

Ranitidine Hydrochloride Insert 1 - Ranitidine Hydrochloride Insert 1

Ranitidine Hydrochloride Insert 1 - Ranitidine Hydrochloride Insert 1

This is a description of a prescription compounding kit containing ranitidine hydrochloride 25.0 mg/mL (equivalent to 22.4 mg/mL ranitidine) in a pineapple/orange oral suspension. The kit includes 6.4 g of ranitidine hydrochloride, 250 mL of oral suspension vehicle, a press-in bottle adaptor, an oral dispenser, and instructions. The kit is manufactured according to US FDA current Good Manufacturing Practice and can only be used for prescription compounding by a licensed medical professional. The pharmacist must remove and inspect the kit contents, wear gloves and eye protection, and follow compounding instructions carefully.*

Ranitidine Hydrochloride Insert 2 - Ranitidine Hydrochloride Insert 2

Ranitidine Hydrochloride Insert 2 - Ranitidine Hydrochloride Insert 2

The text is a set of instructions for mixing a prescription-only oral suspension with ranitidine hydrochloride powder equivalent to 22.4mg/mL ranitidine, into a pineapple/orange flavored vehicle. The final suspension is stable for up to eight weeks and requires re-labeling before use. An oral dispenser is provided. Store the unused kit at room temperature, and the mixed suspension must be stored between 2-8 Celsius.*

Ranitidine Hydrochloride Label - Ranitidine Hydrochloride Label

Ranitidine Hydrochloride Label - Ranitidine Hydrochloride Label

This is a description of a medication called Ranitidine Hydrochloride. It also includes information about the packaging and repackaging company, California Pharmaceuticals, LLC. However, the text appears to have several errors and does not provide clear and coherent information.*

* 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.