Surfs Up Bath Co. Hand Sanitizer
FDA Label NDC 90050-001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Little Bath Co. Llc for the product Surfs Up Bath Co. Hand Sanitizer (NDC 90050-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label - principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 67% v/v.

Purpose

Antiseptic

Use

  • Helps reduce bacteria on the skin.
  • Recommended for repeated use.

Warnings

For external use only.

Flammable, keep away from fire, sparks, and sources of ignition. Do not store above 104°F/40°C.

When using this product Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • For children under 6, use adult supervision.
  • Do not use on infants under 5 months of age.

Inactive Ingredients

Water (Aqua), Aloe Barbadensis Leaf Juice, Hydrolyzed Jojoba Esters, Carbomer, Aminomethyl Propanol, Glycerin, Fragrance (Parfum).

Package Label - Principal Display Panel

Label (Label)

Label (Label)

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