Sea And Ski Coolest Burn Relief
Product Images NDC 73440-2027

9 FDA label images from Cross Brands Contract Filling · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Sea And Ski Coolest Burn Relief (NDC 73440-2027). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cross Brands Contract Filling, 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

9e00ffbf C7d6 176e E053 2a95a90a4c1f

9e00ffbf C7d6 176e E053 2a95a90a4c1f
Drug Facts panel for Sea and Ski Coolest Burn Relief showing active ingredient Lidocaine Hydrochloride 0.5% as a topical anesthetic. It includes uses for temporary relief of pain and itching from sunburn, minor burns, skin irritations, scrapes, and insect bites. Warnings, directions for use, and a list of inactive ingredients are provided. Manufacturer and contact information for Cross-Brands Contract Filling, LLC is visible along with a barcode and a "Made in U.S.A." mark.*
FDA Label Image

Active Ingredients (Active Ingredients)

Active Ingredients (Active Ingredients)
Partial Drug Facts panel from Sea and Ski Coolest Burn Relief showing active ingredient Lidocaine Hydrochloride 0.5% as a topical anesthetic.*
FDA Label Image

Directions (Directions)

Directions (Directions)
The image shows a directions panel for Sea and Ski Coolest Burn Relief, advising adults and children 2 years or older to apply generously to the burned area up to four times daily, with a warning not to use it on children under 2 years without consulting a doctor.*
FDA Label Image

Inactive Ingredients (Inactive Ingredients)

Inactive Ingredients (Inactive Ingredients)
A text panel listing inactive ingredients for a product. Ingredients include acrylates/C10-30 alkyl acrylate crosspolymer, alcohol denatured, algae extract, aloe barbadensis leaf juice, butylene glycol, ethylhexylglycerin, FD&C Blue No. 1, fragrance, glycerin, menthyl lactate, PEG-40 hydrogenated castor oil, phenoxyethanol, polysorbate 20, PPG-26-buteth-26, simmondsia chinensis (jojoba) extract, triethanolamine, and water.*
FDA Label Image

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)

Keep Out Of Reach Of Children (Keep Out Of Reach Of Children)
A warning panel advising to keep the product out of reach of children and instructing to get medical help or contact a Poison Control Center immediately if swallowed.*
FDA Label Image

Purpose (Purpose)

Purpose (Purpose)
Text panel describing Sea and Ski Coolest Burn Relief, stating it soothes and cools burns, scrapes, skin irritations, and insect bites, and is formulated with Lidocaine HCl to aid in pain and itch relief.*
FDA Label Image

Sea& Ski Coolest Burn Relief (Sea Ski Burn Relief Gel 8oz Bk Pa)

Sea& Ski Coolest Burn Relief (Sea Ski Burn Relief Gel 8oz Bk Pa)
Drug Facts panel for Sea and Ski Coolest Burn Relief, a topical anesthetic with 0.5% Lidocaine Hydrochloride active ingredient. The label lists uses for temporary relief of pain and itching from burns, scrapes, skin irritations, and insect bites. It includes warnings, directions for use, inactive ingredients, and manufacturer information for Cross-Brands Contract Filling, LLC.*
FDA Label Image

Usage (Uses)

Usage (Uses)
A drug facts panel section titled 'Uses' describing temporary relief of pain and itching. It states that the product helps relieve and soothe pain from sunburn, minor burns, skin irritations, scrapes, and insect bites.*
FDA Label Image

Warnings (Warnings)

Warnings (Warnings)
Warning and other warnings panel for Sea and Ski Coolest Burn Relief. It includes directions for external use only, cautions to avoid eye contact, and advises stopping use and consulting a doctor if symptoms persist or worsen. It also contains a pregnancy/breast-feeding warning advising consultation with a healthcare professional before use and cautions against excessive use on raw surfaces or blistered areas.*

* 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.