Active Ingredient
ETHYL ALCOHOL 62%
Pure Spring
FDA Label NDC 11822-4660
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rite Aid Corporation for the product Pure Spring (NDC 11822-4660). 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 using this product and ask 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
HELPS REDUCE BACTERIA ON THE SKIN
Warnings
FOR EXTERNAL USE ONLY. FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.
When Using This Product
AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER.
Stop Using This Product And Ask Doctor If
IRRITATION OR REDNESS DEVELOPS AND LASTS.
Keep Out Of Reach Of Children
IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP HELP OR CONTACT A POISON CONTROL IMMEDIATELY.
Directions
WET HANDS THOROUGHLY AND RUB TOGETHER UNTIL DRY.
Other Information
KEEP BELOW 110F (43C)
Inactive Ingredients
WATER (AQUA), PROPYLENE GLYCOL, FRAGRANCE (PARFUM), ACRYLATES /C10-30 ALKYL ACRYLATE CROSSPOLMER, GLYCERIN, ISOPROPYL MYRISTATE, AMINOMETHYL PROPANOL, TOCOPHERYL ACETATE, MANNITOL, CELLULOSE, HYDROXYPROPYL METHYLCELLULOSE,IRON OXIDES (CI77491), RED 4 (CI 14700)
Label Copy
Image Of The Label (Pshssp01)
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