Bitemd Liquid
Product Images NDC 68093-9561

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 14 technical images submitted to the FDA as part of the official labeling for Bitemd (NDC 68093-9561). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wisconsin Pharmacal Company, 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

Package Label (C95614d Label)

Package Label (C95614d Label)
Drug label text panel for BiteMD Insect Bite Relief topical liquid, 0.5 fl oz (14.7 mL) by Wisconsin Pharmacal Company. It includes active ingredients benzocaine 5%, camphor 3%, and phenol 1.35%, directions for use in adults and children 2 years and over, warnings for external use only and to avoid eyes, and manufacturer and distributor information.*
FDA Label Image

Ask Doctor Section (D95614c Ask Dr)

Ask Doctor Section (D95614c Ask Dr)
This text panel provides a warning advising users to stop use and consult a doctor if symptoms worsen, persist for more than 7 days, clear up and recur within a few days, or if use extends longer than one week without doctor guidance.*
FDA Label Image

Package Label (D95614c Card)

Package Label (D95614c Card)
Packaging label for BiteMD Insect Bite Relief topical liquid by Wisconsin Pharmacal Company. The front panel shows 0.5 fl oz (14.7 mL) size, highlighting relief from pain, itching, and infection caused by chiggers, wasps, mosquitoes, and ticks. The back panel includes drug facts, active ingredients benzocaine 5%, camphor 3%, and phenol 1.35%, usage directions, warnings, and manufacturer information.*
FDA Label Image

Instructions For Use Section (D95614c Directions)

Instructions For Use Section (D95614c Directions)
Directions panel for BiteMD Insect Bite Relief topical liquid. Instructions include cleaning the area, applying to the bite by pressing straight down repeatedly until liquid flows, then dabbing sparingly, reapplying in 10 to 15 minutes if itching persists, and removing ticks or bee stingers before treatment.*
FDA Label Image

Do Not Use Section (D95614c Do Not Use)

Do Not Use Section (D95614c Do Not Use)
A product warning panel for BiteMD insect bite relief liquid. It advises users not to get the product in their eyes, not to apply it over large body areas or bandages, and to consult a doctor for deep wounds, animal bites, or serious burns.*
FDA Label Image

Dosage And Administration Section (D95614c Dosage)

Dosage And Administration Section (D95614c Dosage)
This text panel provides usage instructions for BiteMD insect bite relief liquid topical. It advises that adults and children 2 years and older apply the product to the affected area 1 to 3 times daily, while recommending consultation with a doctor for children under 2 years.*
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Inactive Ingredient Section (D95614c Inactives)

Inactive Ingredient Section (D95614c Inactives)
A text panel listing inactive ingredients of the product BiteMD Insect Bite Relief topical liquid, specifically showing Propylene Glycol as one of the inactive ingredients.*
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Purpose Section (D95614c Purpose Section)

Purpose Section (D95614c Purpose Section)
A product text panel for BiteMD insect bite relief liquid, described as an external analgesic and first aid antiseptic. It states that BiteMD begins to work immediately when applied soon after insect bites to counteract effects from a variety of insects including bees, wasps, mosquitoes, ticks, hornets, ants, and more. It also mentions the product is from the makers of Cutter brand.*
FDA Label Image

Questions Section (D95614c Questions)

Questions Section (D95614c Questions)
This image panel contains a customer service contact section titled 'Questions or Comments?' with a toll-free phone number 1-800-767-9927 displayed prominently for consumer inquiries or feedback.*
FDA Label Image

Storage And Handling Section (D95614c Storage)

Storage And Handling Section (D95614c Storage)
This image is a drug facts or text panel titled 'Other Information,' instructing to store the product at room temperature. It includes a single bullet point note regarding storage conditions for the topical liquid insect bite relief product.*
FDA Label Image

Warnings Section (D95614c Warnings)

Warnings Section (D95614c Warnings)
A warning panel for BiteMD insect bite relief liquid topical product. It states the product is for external use only, advises not to get it in eyes, not to apply over large body areas or bandages, and to consult a doctor for deep wounds, animal bites, or serious burns.*
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Active Ingredients (D95614c Active Ingredients)

Active Ingredients (D95614c Active Ingredients)
Drug facts text panel listing active ingredients and their purposes in BiteMD insect bite relief topical liquid: Benzocaine 5% as analgesic, anesthetic, and antipruritic; Camphor 3% as topical analgesic; Phenol 1.35% as first aid antiseptic.*
FDA Label Image

Keep Out Of Reach Of Children Section (D95614c Children)

Keep Out Of Reach Of Children Section (D95614c Children)
A text panel containing safety instructions for a topical insect bite relief product. It advises to keep the product out of reach of children, seek medical help or contact Poison Control if swallowed, and to flush eyes with water for 15 minutes and call a physician if the product gets into the eyes.*
FDA Label Image

Indications And Usage Section (D95614c Indications)

Indications And Usage Section (D95614c Indications)
Drug facts panel from BiteMD Insect Bite Relief topical liquid showing uses, warnings, and precautions. It states the product is for external use only and provides first aid for temporary relief of pain, itching, and infection. Warnings include avoiding eye contact, not applying over large areas or bandages, and consulting a doctor for deep wounds or animal bites.*

* 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.