Hydrophor Ointment
Product Images NDC 71399-5101

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Hydrophor (NDC 71399-5101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akron Pharma 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

Hydrophor100 (Hydrophor100)

Drug Facts panel for HYDROPHOR Ointment 42 g/100g topical ointment by Akron Pharma Inc. Lists Petrolatum 42% as active ingredient for skin protectant use. Includes directions to apply generously to affected areas, warnings for external use only, and storage instructions. Inactive ingredients such as ceresin wax and lanolin alcohol are also noted. Claims to soothe and protect dry skin from chafing and weather effects.*

FDA Label Image

Hydrophor454 (Hydrophor454)

Label for HYDROPHOR Ointment 42 g/100g, a topical human OTC skin protectant by Akron Pharma Inc. The label highlights that it soothes and protects dry skin, with instructions and warnings included. The net weight is 16 oz (454 g), and inactive ingredients such as ceresin wax, lanolin alcohol, mineral oil, paraffin wax, and phenoxyethanol are listed.*

* 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.