Equate Swimmers Instant Ear Dry Liquid
Product Images NDC 49035-989

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Equate Swimmers Instant Ear Dry (NDC 49035-989). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walmart Stores, Inc, 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

Equate Ear Drops Carton

Equate Swimmers Instant Ear Dry Ear Drops label for a 1 FL OZ (30 mL) liquid otic solution. Contains 95% isopropyl alcohol and 5% anhydrous glycerin as active ingredients. The label highlights the product's use as an ear drying aid to clear water from ears after swimming, bathing, or showering, distributed by Walmart Stores, Inc. The packaging includes drug facts, usage directions, warnings, and a barcode.*

FDA Label Image

Equate Ear Drops Label

Drug Facts label for Equate Swimmers Instant Ear Dry Ear Drops, 1 FL OZ (30 mL). It lists the purpose as an ear drying aid with active ingredients isopropyl alcohol 95% in 5% anhydrous glycerin. Usage instructions state it dries water in the ears. Warnings include flammability, avoiding eye contact, and consulting a doctor before use if ear drainage, pain, irritation, or dizziness occur. Directions advise applying 4 to 5 drops per affected ear and storing at room temperature tightly closed.*

FDA Label Image

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Label for Equate Swimmers Instant Ear Dry ear drops, an ear drying aid for swimmers. The label shows 1 FL OZ (30 mL) liquid dosage form, with active ingredients including 95% Isopropyl Alcohol and 5% Anhydrous Glycerin. The product is distributed by Walmart Inc. and is formulated to help prevent water-clogged ears and swimmer's ear discomfort.*

* 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.