Annie
FDA Label NDC 75629-750

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Annie International, Inc for the product Annie (NDC 75629-750). 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, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Active Ingredient

→ Purpose

→ Use

→ Warnings

→ When Using This Product

→ Stop Use And Ask A Doctor If

→ Keep Out Of Reach Of Children.

→ Directions

→ Other Information

→ Inactive Ingredients

→ Principal Display Panel

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

Use

Hand Sanitizer to help reduce bacteria on the skin

Warnings

For external use only. Do not drink.

Flammable. Keep away from fire or flame

Avoid contact with broken skin

When Using This Product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor If

irritation or rash appears and lasts

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Not recommended for infants

Directions

Apply the sanitizer to the palm of one hand and rub all over hands until your hands are dry
Children under 6 years of age should be supervised when using

Other Information

Store below 110°F (43°C)
May discolor certain fabrics or surfaces

Inactive Ingredients

Water (Aqua), Aloe Barbadensis Leaf Juice, Maltodextrin, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Fragrance, Tocopheryl Acetate.