Butalbital, Aspirin And Caffeine
Product Images NDC 21695-354

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Butalbital, Aspirin And Caffeine (NDC 21695-354). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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

Structural Formula For Butalbital (4e10129b 41a3 4572 9564 6f8366b627dc 01)

Chemical structure of the active ingredient Butalbital, Aspirin and Caffeine combination product. The image depicts molecular bonds and atom groups characteristic of these compounds.*

FDA Label Image

Structural Formula For Aspirin (4e10129b 41a3 4572 9564 6f8366b627dc 02)

Chemical structure diagram showing a benzene ring with two substituents: a carboxylic acid group (COOH) and a methoxycarbonyl group (OCOCH3). This represents the chemical structure depicted in the image.*

FDA Label Image

Structural Formula For Caffeine (4e10129b 41a3 4572 9564 6f8366b627dc 03)

Chemical structure diagram of the active ingredient shown in the product Butalbital, Aspirin and Caffeine. The structure depicts the molecular arrangement of atoms in the caffeine compound.*

FDA Label Image

Butalb/asa/caffeine 50/325/40mg (4e10129b 41a3 4572 9564 6f8366b627dc 04)

Label for Butalbital, Aspirin and Caffeine tablets, strength 50 mg / 325 mg / 40 mg, bottle count #60. Label includes NDC 21695-354-60 and indicates the product is manufactured by West-ward Pharmaceutical Corp., Eaton, NJ. Packaged by Physician Partner, Thousand Oaks, CA. The label provides standard packaging and storage 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.