Pain Relief Pm Tablet
Product Images NDC 55910-834

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pain Relief Pm (NDC 55910-834). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dolgencorp, 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.

FDA Label Image

Dg-apappm-100ct-ifc (Dg Apappm 100ct Ifc)

Dg-apappm-100ct-ifc (Dg Apappm 100ct Ifc)
This text appears to be the description and drug facts for a product called "Varnish Omit." It is a pain reliever containing Acetaminophen (500 mg) and Diphenhydramine HCI (25 mg), which is a nighttime sleep aid. It is indicated for temporary relief of occasional headaches and minor aches and pains with accompanying sleeplessness. The product contains warnings regarding liver damage if more than 4,000 mg of acetaminophen is taken in 24 hours and if taken with other drugs containing acetaminophen or with alcohol. It also warns of possible allergic skin reactions and advises against use with other products containing acetaminophen or diphenhydramine, in children under 12 years of age, and if there has been an allergic reaction to the product or any of its ingredients in the past. It further advises consulting a doctor before use in cases of liver disease, breathing problems, trouble urinating, or glaucoma. The product may cause drowsiness and caution should be taken when operating machinery or driving. If sleeplessness persists for more than 2 weeks or if pain or fever worsens or other symptoms occur, medical attention should be sought. The product should not be used by pregnant or breastfeeding women without consulting a healthcare professional. Keep out of reach of children. In case of overdose, medical help should be sought immediately. The product comes in the form of caplets, and the recommended dosage for adults and children 12 years and over is 2 caplets at bedtime, not to exceed 2 caplets in 24 hours. The inactive ingredients include carnauba wax, colloidal silicon dioxide, FD&C blue #1 aluminum lake, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, pregelatinized starch, sodium starch glycolate, stearic acid, talc, and titanium dioxide. The product is distributed by Old East Main Co. and offers 100% satisfaction guaranteed with customer service contact information provided. The text also includes a tamper-evident warning and the ingredients of Extra Strength Tylenol PM Caplets.*
FDA Label Image

Dg-apappm-100ct-label (Dg Apappm 100ct Label)

FDA Label Image

Dg-apappm-50ct-ifc (Dg Apappm 50ct Ifc)

Dg-apappm-50ct-ifc (Dg Apappm 50ct Ifc)
This text appears to be the description of a medication product. The product is a combination of acetaminophen and diphenhydramine, which is used for temporary relief of occasional headaches and minor aches and pains with accompanying sleeplessness. It is a pain reliever and nighttime sleep aid. The text provides warnings and directions for use, including information about potential side effects and interactions with other medications. It is important to read the complete warnings and product information on the carton. The text also includes contact information for any questions or comments regarding the product.*
FDA Label Image

Dg-apappm-50ct-label (Dg Apappm 50ct Label)

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