Sunmark Isopropyl Alcohol 70 Percent With Wintergreen Oil Liquid
Product Images NDC 49348-175

2 FDA label images from Strategic Sourcing Services 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 Sunmark Isopropyl Alcohol 70 Percent With Wintergreen Oil (NDC 49348-175). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strategic Sourcing Services 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

Sm70w.jpg (Sm70w)

Sm70w.jpg (Sm70w)
Sunmark Isopropyl Alcohol 70 Percent With Wintergreen Oil topical liquid, 16 FL OZ (473 mL) bottle label. The label highlights 70% USP isopropyl rubbing alcohol with wintergreen for rubbing, massaging, and sponge baths. Distributed by McKesson, it includes drug facts, warnings, directions, and inactive ingredients.*
FDA Label Image

Principal Display Panelndc 49348-175-38isopropylrubbingalcohol70% Uspwintergreen16 Fl Oz (1 Pt) 473 mL (Sunmark Isopropyl Alcohol 70 Percent Usp With Wint 01)

Principal Display Panelndc 49348-175-38isopropylrubbingalcohol70% Uspwintergreen16 Fl Oz (1 Pt) 473 mL (Sunmark Isopropyl Alcohol 70 Percent Usp With Wint 01)
The label for Sunmark Isopropyl Alcohol 70 Percent With Wintergreen Oil liquid displays the brand name, active ingredient as isopropyl alcohol 70% USP, and strength. The label highlights the wintergreen scent and the volume of 16 fluid ounces (473 mL). It includes warnings, directions, inactive ingredients, and distributor information from McKesson. The label also shows the NDC number 49348-175-38 and a barcode.*

* 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.