Active Ingredient(S)
Alcohol 75% Purpose: Antiseptic
Popcare
FDA Label NDC 81478-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo The One Bio-technology Co., Ltd for the product Popcare (NDC 81478-001). 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(s), purpose, use, warnings, otc - when using, otc - stop use, otc - 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
Use
Hand sanitizer to help reduce bacteria on the skin.
Warnings
For external use only. Flammable. Keep away from heat or flame
Otc - When Using
When using the product
Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Avoid contact with broken skin.
Otc - Stop Use
Stop use and ask a doctor
if irritation or redness develops condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Lift tab at front of the lid to open.
Pull up corner of center sheet and thread through dispenser slit in the lid.
Pull up exposed wipe and snap off.
The next wipe is ready for dispensing.
Close lid to retaining moisture. T
ake wipe and rub thoroughly over all surfaces of both hands. Rub hands briskly together to dry.
Dispose of used wipe in trash.
Do not Flush.
Not recommended for infants
Other Information
Do not store above 105F/40C
May discolor some fabrics
Harmful to wooden finishes and plastics
Inactive Ingredients
R0 puter water
* Please review the disclaimer below.
