Otc - Active Ingredient
Active Ingredient Purpose
Ethyl Alcohol 62% Antiseptic
Hand Sanitizer Spray
FDA Label NDC 42681-0009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Whole Foods Market, Inc. for the product Hand Sanitizer (NDC 42681-0009). 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 otc - active ingredient, otc - purpose, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Uses ■ to help reduce bacteria on the skin.
Warnings
For external use only. Flammable. Keep away from fire or flame.
Otc - When Using
When using this product avoid contact with eyes. If eye contact occurs, rinse with water.
Otc - Stop Use
Stop use and ask a doctor if skin irritation or redness develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.
Dosage & Administration
Directions ■ apply 1 to 2 sprays on hands and rub together until dry.
Storage And Handling
Other information ■ do not store above 104°F (40°C).
Inactive Ingredient
Inactive ingredients water, isopropyl alcohol, glycerin, fragrance (natural)*, helianthus annuus (sunflower) seed oil, rosmarinus officinalis (rosemary) leaf extract, triethyl citrate.
*Complies with ISO 9235, see www.wholefoodsmarket.com for more information.
Otc - Questions
Questions, Comments? ■ [email protected] ■ 1-844-936-8255
Package Label.Principal Display Panel
Cas2 (Cas2)
* Please review the disclaimer below.
