K-mart Smartsense First Aid Contains 303 Pieces
Product Images NDC 49738-802

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for K-mart Smartsense First Aid Contains 303 Pieces (NDC 49738-802). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kmart Corporation, 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

Alcoholcleansingpad (Alcoholcleansingpad)

Drug Facts panel for Alcohol Cleansing Pad including active ingredient (Isopropyl Alcohol, 70% v/v), intended use as antiseptic, warnings for external use only and keeping away from fire, directions to wipe injection site vigorously and discard, storage instructions, and lot/expiration information. The label is bilingual in English and Spanish and includes manufacturer details for Genuine First Aid LLC.*

FDA Label Image

Antiseptic Towelette (Antiseptictowelette)

Label for K-Mart SmartSense First Aid Antiseptic Towelettes, bilingual English and Spanish text. It features product identification, reorder number AST-001, standard compliance logos including CE and ISO 9001:2010, manufacturer Genuine First Aid LLC in Clearwater, Florida, and indicates one towelette per pouch.*

FDA Label Image

Burncream (Burncream)

Drug Facts panel for Genuine First Aid Burn Cream, indicating it is an antiseptic pain relief cream with aloe containing active ingredients benzalkonium chloride 0.13% and lidocaine HCL 0.5%. The label provides purpose, uses, warnings, directions, and storage instructions, along with manufacturing information.*

FDA Label Image

Chewable Aspirin 81mg (Chewableaspirin)

Drug Facts panel for Genuine First Aid Chewable Aspirin 81 mg tablets. It details the active ingredient aspirin as analgesic/antipyretic, uses for minor aches and fever reduction, warnings including Reye's syndrome, stomach bleeding, allergy precautions, pregnancy warnings, dosage directions for adults and children, storage instructions, and a list of inactive ingredients. Distributed by Genuine First Aid in Clearwater, FL.*

FDA Label Image

Genuineeyewash (Genuineeyewash)

Label for a 10 ml sterile isotonic buffered eyewash solution labeled as 'GENUINE Eyewash' for single use only. The label includes directions for use, lists the active ingredient as purified water, and several inactive ingredients. It states the product is for irrigation only, not for injection, and includes manufacturer details indicating it is made in India for Genuine First Aid.*

FDA Label Image

Genuinetripleantibiotic (Genuinetripleantibiotic)

Drug Facts panel for Genuine Triple Antibiotic First Aid Ointment displaying uses, warnings, directions, and storage information. The ointment contains Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate, and instructions caution external use only with directions for application and advice to consult a doctor if adverse reactions occur.*

FDA Label Image

Insect Sting Relief Pad (Insectstingreliefpad)

Drug Facts panel for Insect Sting Relief Pad showing active ingredient benzocaine 6% w/w, purpose as topical anesthetic, and uses including temporary relief of pain and itching from insect bites. Includes warnings, directions, and bilingual labeling in English and Spanish. Manufactured by Genuine First Aid LLC, Clearwater FL.*

FDA Label Image

K Mart Smartsense Kit 303 (Km R303)

Packaging label for K-Mart SmartSense First Aid Kit containing 303 pieces. The label highlights key features such as a six-pocket kit for cleaning and treating small or medium cuts and scratches, severe bleeding and burns, and including a CPR breathing barrier. The labeler is Kmart Corporation. The packaging is predominantly red with white and orange text and includes images of people 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.