Acetaminophen 500mg Diphenhydramine Hcl 25mg
Product Images NDC 70692-119

3 FDA label images from Strive Pharmaceuticals Inc · 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 Acetaminophen 500mg Diphenhydramine Hcl 25mg (NDC 70692-119). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strive Pharmaceuticals 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

Ct11905

Ct11905
Packaging label for Pain Relief PM Extra Strength caplets containing acetaminophen 500mg and diphenhydramine HCl 25mg, distributed by Strive Pharmaceuticals Inc. The label shows 50 caplets, identifies the product as a pain reliever and nighttime sleep aid, and includes Drug Facts with active ingredients and warnings.*
FDA Label Image

Ct11941 (Ct11941)

Ct11941 (Ct11941)
Packaging label for SoloPara PM Acetaminophen 500mg Diphenhydramine HCl 25mg caplets by Strive Pharmaceuticals Inc. The green label shows the product name, active ingredients and strength, with a body pain graphic. The package contains 4 caplets and includes detailed drug facts, usage warnings, directions, lot and expiration date sections.*
FDA Label Image

Lb11905

Lb11905
Drug Facts panel for Acetaminophen 500mg Diphenhydramine HCl 25mg caplets by Strive Pharmaceuticals Inc. It lists active ingredients, uses, warnings, directions for use, storage information, and contact information for questions or comments. The panel highlights the product as an extra strength pain reliever and nighttime sleep aid.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.