Otc - Active Ingredient
Alcohol 77%
Antacgel
FDA Label NDC 79633-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Medipharco Pharmaceutical Joint Stock Company for the product Antacgel (NDC 79633-101). 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, indications & usage, warnings, otc - do not use, otc - when using, otc - stop use, otc - 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
Otc - Purpose
Antiseptic
Indications & Usage
Hand sanitizer spray helps to sanitize hands, eliminate unpleasant odor and leave hands feeling soft and fresh.
Warnings
For external use only. Flammable. Keep away from the heat or flame.
Otc - Do Not Use
* in children less than 2 months of age
* on open skin wounds
Otc - When Using
keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Otc - Stop Use
if irritation or rash occurs. These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Storage And Handling
* Spray the solution to one hand. Thoroughly rub your hands together until dry.
* Supervise children under 6 years of age when using this product to avoid swallowing.
* Store below 86°F (30°C)
* May discolor certain fabrics or surfaces
Inactive Ingredient
Isopropyl myristate, Orange oil, Peppermint oil, Purified Water, Yellow (C.I. 15985)
Dosage & Administration
Spray the solution to one hand. Thoroughly rub your hands together until dry.
* Please review the disclaimer below.
