Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer Gel
FDA Label NDC 42681-7162
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 42681-7162). 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, indications & usage, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antiseptic
Warnings
For external use only. Flammable. Keep away from fire or flame.
Otc - When Using
When using this productavoid contact with eyes. If eye contact occurs, rinse with water.
Otc - Stop Use
Stop use and ask a doctor ifskin 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.
Indications & Usage
Usesto help reduce bacteria on the skin
Dosage & Administration
Directionsapply enough gel to wet hands and rub together until dry. Use 1 to 3 times daily.
Storage And Handling
Other informationdo not store above 104°F (40°C).
Otc - Questions
Inactive Ingredient
Inactive ingredientswater, isopropyl alcohol, hydroxyethylcellulose, salvia hispanica (chia) seed oil, glycerin, helianthus annuus (sunflower) seed oil, rosmarinus officinalis (rosemary) leaf extract, fragrance (natural)*, polysorbate 20.
*Complies with ISO 9235, see www.wholefoodsmarket.com for more information.
Package Label.Principal Display Panel
Lg32 (Lg32)
* Please review the disclaimer below.
