Red Chilli Plaster
Product Images NDC 72335-100

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Red Chilli Plaster (NDC 72335-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Trinet Industries 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

6f04fa54 7f44 Be2d E053 2a91aa0ac697

Packaging label for Red Chilli Plaster by Trinet Industries Inc, distributed by K-ONE CO., made in Korea. The label features the product name in English and Chinese, an illustration of red chili peppers with flowers, and specifies dimensions of 124mm x 168mm with 1 piece per package. The NDC number 72335-100-01 is shown along with the distributor's address in LA, CA.*

FDA Label Image

Red Chilli (Red Chilli Draft Label With Dfp Rev1)

Drug Facts panels for Red Chilli Plaster by Trinet Industries Inc include active ingredients methyl salicylate (0.64%), camphor (0.55%), and capsicum (2.33%) listed as topical analgesics. The panels detail uses for temporary relief of minor aches and pains associated with arthritis, simple backache, strains, bruises, and sprains. Warnings emphasize external use only, avoiding damaged skin, eyes, and mucous membranes, and consulting a doctor for allergic reactions or prolonged symptoms. Directions specify application 3 to 4 times daily for 7 days on adults and children 12 years and older, with instructions to consult a doctor for younger children. Additional information notes potential latex allergy and storage precautions. Inactive ingredients and distributor contact information are also included.*

* 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.