Refreshify Antiseptic Hand Wipes
Refreshify Antiseptic Hand Wipes
Approved
Approval ID
d2c4e1cc-58c5-4af8-9ac0-8af3b37373a1
Product Type
HUMAN OTC DRUG LABEL
Effective Date
Aug 19, 2025
Manufacturers
FDA
Emes Commerce Group Inc.
DUNS: 026815145
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
ALCOHOL
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code87031-000
Application Number505G(a)(3)
Product Classification
M
Marketing Category
C200263
G
Generic Name
ALCOHOL
Product Specifications
Effective DateAugust 19, 2025
FDA Product Classification
Drug Labeling Information
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
LOINC: 51945-4Updated: 8/1/2025
Kit label
INDICATIONS & USAGE SECTION
LOINC: 34067-9Updated: 8/19/2025
Use
for hand washing to decrease bacteria on the skin.
SPL UNCLASSIFIED SECTION
LOINC: 42229-5Updated: 8/19/2025
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
LOINC: 55106-9Updated: 8/19/2025
Active ingredient
Ethyl alcohol 75%
Purpose
Antiseptic
WARNINGS SECTION
LOINC: 34071-1Updated: 8/19/2025
Warnings
For external use only
Flammable, keep away from fire or flame.
Do not use
- in the eyes
Stop use and ask a doctor if
- irritation and redness develop
- condition persists for more than 72 hours
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
LOINC: 34068-7Updated: 8/19/2025
Directions
Wet hands thoroughly with wipe and allow to dry without wiping.
INACTIVE INGREDIENT SECTION
LOINC: 51727-6Updated: 8/19/2025
Inactive ingredient
Water (Aqua)