Ibuprofen And Diphenhydramine Citrate Tablet, Coated
Product Images NDC 21130-228

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ibuprofen And Diphenhydramine Citrate (NDC 21130-228). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Better Living Brands, Llc, 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

Package Label-principal Display Panel (200 mg/38 mg (20 Coated Caplets) Bottle Label)

Package Label-principal Display Panel (200 mg/38 mg (20 Coated Caplets) Bottle Label)
Drug Facts label panel for Ibuprofen and Diphenhydramine Citrate Tablets 200 mg/38 mg by Better Living Brands, LLC. The label includes active ingredient information, purposes, warnings, usage directions, and storage instructions across multiple folds labeled as Top Ply and Bottom Ply, detailing comprehensive safety and usage guidelines for this coated oral tablet combination of pain reliever and nighttime sleep-aid.*
FDA Label Image

Package Label-principal Display Panel (200 mg/38 mg (20 Coated Caplets) Bottle Carton Label)

Package Label-principal Display Panel (200 mg/38 mg (20 Coated Caplets) Bottle Carton Label)
Flat packaging label for Ibuprofen and Diphenhydramine Citrate Tablets 200 mg/38 mg by Better Living Brands, LLC. Coated tablets for oral use, 20 count per box. The label includes Drug Facts, directions, warnings, active and inactive ingredients, barcode, and manufacturer/distributor information. The label cautions about allergy warnings, usage instructions, and safety information.*

* 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.