Theraflu Powder, For Solution
Product Images NDC 0067-7918

2 FDA label images from Haleon Us Holdings Llc · 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 Theraflu (NDC 0067-7918). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Haleon Us Holdings 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

13215_theraflu Ms Sc & Theraflu Nt Scc Combo_12 Ct.jpg (Image 01)

13215_theraflu Ms Sc & Theraflu Nt Scc Combo_12 Ct.jpg (Image 01)
The label for THERAFLU NIGHTTIME SEVERE COLD AND COUGH powder for solution shows a dual panel design highlighting two formulations: Multi-Symptom Severe Cold and Severe Cold & Cough. Active ingredients include acetaminophen, diphenhydramine HCl, and phenylephrine HCl. The nighttime variant is honey lemon flavored with chamomile and white tea, while the multi-symptom variant features green tea and honey lemon. The box contains 12 packets total, divided as 6 multi-symptom and 6 nighttime packets, produced by Haleon US Holdings LLC.*
FDA Label Image

Image 02

Image 02
THERAFLU NIGHTTIME SEVERE COLD AND COUGH powder for solution label showing multi-symptom severe cold and severe cold & cough formulas. Active ingredients listed include acetaminophen, diphenhydramine HCl, and phenylephrine HCl for nighttime use. The label highlights 24 total packets, with 18 multi-symptom and 6 nighttime packets, featuring tea infusions with green tea, honey lemon, camomile, and white tea flavors. Brand and GSK logo appear on a blue and yellow background.*

* 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.