Gniby - Lidocaine Anorectal Hemorrhoidal Cream
Product Images NDC 87152-002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Gniby - Lidocaine Anorectal Hemorrhoidal (NDC 87152-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Putian Licheng District Zhijiancheng Trading Co., Ltd., 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

Labeling (87152 002 01 50g)

Gniby Numbing Cream 5% Lidocaine anorectal (hemorrhoidal) topical cream, net weight 1.75 oz (50g). The black label features gold decorative elements and text highlighting numbing effect and maximum strength for long-lasting relief. Distributed by HSIERQ Trading Ltd., made in PRC. Active ingredient and inactive ingredients listed; usage, warnings, directions, and storage instructions appear on the label.*

FDA Label Image

Labeling-60 (87152 002 02 60g)

Label for Gniby Numbing Cream, an anorectal (hemorrhoidal) topical cream containing 5% lidocaine. The net weight is 2 oz (60 g). The label features a black background with gold ornate detailing and includes Drug Facts, active and inactive ingredients, warnings, usage directions, storage instructions, and contact information. The product is distributed by HSIERQ Trading Ltd, designed in the USA, and made in PRC.*

FDA Label Image

Labeling-30 (87152 002 03 30g)

Packaging label for Gniby Numbing Cream containing 5% lidocaine, a topical anesthetic for anorectal (hemorrhoidal) use. The product is for external use only, with a net weight of 1.1 oz (30g). Label includes active and inactive ingredients, usage directions, warnings, and storage information. Distributed by HSIERQ Trading Ltd, made in PRC.*

* 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.