Hand Sanitizer Spray
Product Images NDC 87001-005

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 87001-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Haian Kangrui Textile 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

3 (Es 0)

3 (Es 0)
Drug Facts label for Hand Sanitizer spray with ethyl alcohol 70% v/v as the active ingredient. The label includes sections for uses, directions, inactive ingredients, warnings, and storage instructions. It notes the product is flammable and for external use only. The label also contains product weight (1.18 oz, 35 ml) and states it is made in China.*
FDA Label Image

87001-005-01(1) (O 2)

87001-005-01(1) (O 2)
Packaging label for Moisturizing Hand Sanitizer spray with Citrus scent, containing 1.18 fl. oz. (35 mL). The active ingredient is Ethyl Alcohol 70% v/v. The label is orange with white and black text. It includes Drug Facts, warnings, directions, and inactive ingredients. Manufactured by HAIAN KANGRUI TEXTILE CO., LTD. and made in China.*
FDA Label Image

87001-005-01(2) (P 3)

87001-005-01(2) (P 3)
Packaging label for Hand Sanitizer spray containing Ethyl Alcohol 70% v/v. The front panel shows the product is moisturizing with a lavender scent and 1.18 fl. oz. (35 mL) volume. The back panel includes Drug Facts with active/inactive ingredients, usage warnings, directions, storage information, hazard symbols, a barcode, and a contact number. The labeler is HAIAN KANGRUI TEXTILE CO., LTD.*

* 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.