Active Ingredient
Alcohol 80% v/v
Doctor Safe
FDA Label NDC 78542-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by One Diamond Electronics, Inc. for the product Doctor Safe (NDC 78542-001). 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, warnings, uses, directions, keep out of reach of children., other information, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Warnings
For external use only. Flammable. Keep away from heat or flame.
Do not use:
1) in children less than 2 months of age;
2) on open skin wounds.
When using this product keep out of eyes, ears, and mouth.
In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs.
These may be signs of a serious condition.
If swallowed, get medical help, or contact a Poison Control Center right away.
Uses
Hand Sanitizer to help reduce bacteria that potentially can cause disease.
For use when soap and water are not available.
Directions
1) Place enough product on hands to cover all surfaces. Rub hands together until dry;
2) Supervise children under 6 years of age when using this product to avoid swallowing.
Keep Out Of Reach Of Children.
If swallowed, get medical help, or contact a Poison Control Center right away
Other Information
1) Store between 15-30C (59-86F);
2)Avoid freezing and excessive heat above 40C (104F
Inactive Ingredient
Glycerin, Hydrogen peroxide, Purified water USP.
1.5Ml
Image Description (1.5ml)
6Packs
Image Description (2oz)
59Ml Bottle
Image Description (59ml)
236Ml
Image Description (236ml)
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