Hand Sanitizer
FDA Label NDC 74979-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Robert Gordon Ind. Ltd. for the product Hand Sanitizer (NDC 74979-002). 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 drug facts, active ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Alcohol 75 %
Purpose
Antiseptic
Use
- For handwashing to decrease bacteria on the skin
Warnings
For external use only
- Flammable, keep away from fire and flame
- Does not contain grain alcohol; do not drink if taken internally will produce serious gastric distric disturbances.
When Using This Product
- Avoid the eyes and mucous membranes
- In the case of eyes or mucous membranes contact, rinse area thoroughly with water
Stop Use And Ask A Doctor If
- Condition worsens
- Redness or irritation develops
- Condition persists for more than 3 days
Keep Out Of Reach Of Children
- If swallowed,contact a doctor or Poison Control Center immediately.
Directions
- Rub dime sized amount between hands until dry.
- Supervise children in the use of this product.
- In the case of eye contact, rinse eyes thoroughly with water.
Other Information
- Store below 105 °F
- May discolor some fabrics.
Inactive Ingredients
Water,Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol.
Questions?
- 516-354-8888
Package Labeling: 100Ml
Bottle (Bottle)
Package Labeling:250Ml
Bottle2 (Bottle2)
Package Labeling:500Ml
Bottle3 (Bottle3)
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