Active Ingredient
Ethyl Alcohol 75%
Orchard Hand Sanitizer
FDA Label NDC 74935-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Orchard Aromatherapy & Skin Care Co.,ltd for the product Orchard Hand Sanitizer (NDC 74935-006). 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, uses, 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
Purpose
Antiseptic
Uses
- For hand sanitizing to decrease bacteria on the skin
- Recommended for repeated use
Warnings
For external use only
When Using This Product:
avoid contact with eyes. In case of eye contact, flush eyes with water.
Stop Use And Ask A Doctor If:
irritation or redness develops, or if condition persist for more than 72 hours.
Keep Out Of Reach Of Children.
If swallowed get medical help or contact a Poison Control Center right away.
Directions
Squeeze appropriate amount of sanitizer on to hands and rub together until dry. Use as needed. For children under 6, use with adult supervision. Not recommended for infants.
Inactive Ingredients:
Water, Aloe Barbadensis Leaf Extract, Acrylate/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine
Package Labeling: 500Ml
Label (Label)
Package Labeling: 60Ml
Label2 (Label2)
Package Labeling: 120Ml
Label3 (Label3)
Package Labeling: 250Ml
Label4 (Label4)
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