Anti-itch Cream
Product Images NDC 84051-001

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Anti-itch Cream (NDC 84051-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Buzzie 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

Directions (Buzzie Dosage Directions Section)

Directions for Anti-Itch Cream topical use instruct adults and children 2 years and older to apply a thin layer on clean skin to the affected area. It advises letting the cream absorb without rubbing, applying at symptom onset, not more than 6 times per day or every 15 minutes for the first hour, and avoiding use with other topical remedies or lotions.*

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Inactive Ingredients (Buzzie Inactive Ingredients Section)

This image shows the inactive ingredients list of a topical cream product. Ingredients include Adansonia Digitata (Baobab) Seed Oil, Aqua/Water, Butylene Glycol & Chenopodium Quinoa Seed, Citric Acid, Cross-linked acrylic acid homopolymer, Ethyl Alcohol, Mentha Piperita Oil, Methyl Glucose Dioleate, and Sodium Hydroxide.*

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Other Information (Buzzie Other Information Section)

This image shows a continuation of the Drug Facts panel for Anti-Itch Cream. It provides additional storage instructions advising to store the product in a cool, dark place away from children, avoid direct sunlight, and use only if the tamper-evident safety seal is intact for protection.*

FDA Label Image

Front Panel (Buzzie Principal Display Panel)

Label of Buzzie Anti-Itch Cream, showing a 0.53 oz (15 gm) topical cream with plant-powered ingredients. The label states 'Family Friendly' and features a bee logo above the brand name Buzzie. The phrase 'The best places in the world are full of bugs' is also displayed.*

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Purpose Section (Buzzie Purpose Section)

Drug Facts text panel from Anti-Itch Cream by Buzzie LLC. The visible section lists the product's purpose, including anti-inflammatory, anti-itching for burning and analgesic relief, focusing on symptoms like mild skin irritation, burning, and stinging.*

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Question Section (Buzzie Questions Section)

A text snippet from the product labeling of Anti-Itch Cream by Buzzie LLC, showing a customer service prompt: "Questions or Comments? Visit us at Buzzie.com." This appears to be part of the contact or support information section.*

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Uses Section (Buzzie Uses Section)

This text panel explains that the Anti-Itch Cream is used for temporary relief of inflammation, pain, itching, burning, and stinging sensations based on Homeopathic Materia Medica. It also states that product efficacy and claims are based on homeopathy theories not supported by scientific evidence or most allopathic medical professionals.*

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Warning Section (Buzzie Warnings Section)

Drug Facts panel continuing with warnings for Anti-Itch Cream. It includes instructions for external use only, avoiding damaged or broken skin, keeping out of eyes, wounds, and mucous membranes, and guidance to stop use and ask a physician if conditions worsen. It advises consulting a doctor if pregnant or breastfeeding, and keeping the product out of reach of children with emergency instructions if swallowed.*

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Active Ingredients (Active Converted)

Drug Facts panel listing active ingredients and purposes for Anti-Itch Cream. Ingredients include Althaea Officinalis 1X, Arnica Montana 1X, Hypericum Perforatum 1X, Lycopodium Clavatum 1X, Mezereum 4X, Sabina 3X, and Urtica Urens 1X. Purposes stated are anti-inflammatory, anti-itching and burning, analgesic, and relieve itching, burning, and stinging. Notes that active ingredients are HPUS (Homeopathic Pharmacopoeia of the United States).*

* 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.