Alcohol Prep Pad Swab
Product Images NDC 71412-110

7 FDA label images from R&c Imports Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Alcohol Prep Pad (NDC 71412-110). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by R&c Imports 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

Back Box (Printing Marks Alcohol Pad Back Box)

Back Box (Printing Marks Alcohol Pad Back Box)
This Drug Facts panel for Alcohol Prep Pad with 70% Isopropyl Alcohol details active and inactive ingredients, use directions, warnings including flammability and external use only, storage instructions, and manufacturer information. It notes the product is sterile unless opened, not made with natural rubber latex, and the packaging contains 200 medium-sized pads.*
FDA Label Image

Box Front (Printing Marks Alcohol Pad Front Box)

Box Front (Printing Marks Alcohol Pad Front Box)
Alcohol Prep Pad Sterile containing 70% Isopropyl Alcohol, single-use swabs saturated with 0.7 mL each. The label states topical application, discard after use, and that it is not made with natural rubber latex. Pack contains 200 medium-sized pads, labeled by R&C Imports LLC with NDC 71412-110-20.*
FDA Label Image
Side Box (Printing Marks Alcohol Pad Side Box)
Alcohol Prep Pad Sterile packaging label for isopropyl alcohol swabs saturated with 70% isopropyl alcohol. The label indicates topical application, single use discard, and that the product is not made with natural rubber latex. The container holds 200 medium-sized pads. The labeler is R&C Imports LLC, with NDC 71412-110-20 shown.*
FDA Label Image

Inner Back Box (Back Box)

Inner Back Box (Back Box)
Drug Facts panel for Alcohol Prep Pad containing Isopropyl Alcohol 70% v/v as the active antiseptic ingredient. Includes usage instructions for skin preparation prior to injection, warnings about external use, flammability, and keeping out of children's reach. Directions indicate applying alcohol as needed and discarding after single use. Also notes inactive ingredient purified water, manufacturing details, and storage cautions including sterility and latex information. Package contains 200 medium pads and is made in India.*
FDA Label Image

New Box Pre Pad Front (Box Alcohol Pre Pad Art 2)

New Box Pre Pad Front (Box Alcohol Pre Pad Art 2)
Packaging label for AXISCARE Alcohol Prep Pad Sterile swabs, medium size, containing 200 pads. Each pad is saturated with 70% isopropyl alcohol. Label notes single-use, topical application, and that pads are not made with natural rubber latex. Labeler is R&C Imports LLC with product NDC 71412-110-20.*
FDA Label Image

New Box Alcohol Prep Pad Back Art (Box Alcohol Pre Pad Back Art 2)

New Box Alcohol Prep Pad Back Art (Box Alcohol Pre Pad Back Art 2)
The image shows the back label of an Alcohol Prep Pad swab package containing 200 pads, with active ingredient isopropyl alcohol 70%. It includes usage instructions, warnings, and storage information, stating it is sterile unless opened or damaged and not made with natural rubber latex. The label identifies R&C Imports LLC as the labeler and indicates the product is made in China.*
FDA Label Image

Inner Front Box (Front Box)

Inner Front Box (Front Box)
Packaging label for Axiscare Alcohol Prep Pad, saturated with 70% isopropyl alcohol. The product is sterile and not made with natural rubber latex. The label indicates 200 pieces and includes item number APS-M4000. The labeler is R&C Imports LLC, with NDC 71412-110.*

* 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.