Buscapina Tablet, Coated
Product Images NDC 69729-131

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Buscapina (NDC 69729-131). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Opmx 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

Carton (Buscapina Carton)

Buscapina coated tablets packaging label featuring Acetaminophen 500 mg, Caffeine 60 mg, and Pyrilamine Maleate 15 mg per tablet. The label shows the brand and ingredients prominently with bilingual symptom relief indications including cramps, bloating, fatigue, headache, and backache. It also lists package details as 144 caplets and 72 packs of 2 caplets. The labeler is OPMX LLC.*

FDA Label Image

Packet (Buscapina Label)

Buscapina coated tablets containing Acetaminophen 500 mg, Caffeine 60 mg, and Pyrilamine Maleate 15 mg per caplet. The label highlights uses for relief of menstrual cramps, bloating, fatigue, headache, and backache. It indicates a package size of 2 caplets and shows warnings, directions, and storage information. Manufactured by OPMX LLC, with branding and a tamper-evident notice.*

FDA Label Image

B100 (Buscapina Display100rev)

Buscapina medication packaging label for coated tablets with active ingredients acetaminophen 500 mg, caffeine 60 mg, and pyrilamine maleate 15 mg. The label includes bilingual text in English and Spanish, listing product purposes and uses for pain relief, cramps, bloating, fatigue, and backache associated with menstrual periods. The box contains 100 caplets in 50 packs of 2 caplets each. It is labeled by OPMX LLC, with usage instructions, warnings, and additional product information provided on the label.*

* 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.