Inactive Ingredient
Inactive Ingredients
Water, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,
Triethonalamine, Fragrance, PEG-40 Hydrogenated
Castor Oil, May contain:
D C Red 33, FD C Red 4, FD C Yellow 5, FD C Blue 1
Spatheraphy
FDA Label NDC 56136-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Xiamen Olivee Daily Use Chemical Co., Ltd. for the product Spatheraphy (NDC 56136-005). 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 inactive ingredient, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, otc - stop use, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Active Ingredient
Alcohol Denat 62 % w/w
Otc - Purpose
Purpose
Antibacterial
Indications & Usage
Use
-To decrease bacteria on the skin and clean hands
-Recommended for repeated use
Warnings
Warnings
For external use only
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
If accidentally swallowed, get medical help or
contact a Poison Control Center right away.
Otc - Stop Use
Discontinue use if irritation or redness develop. If irritation persists
for more than 72 hours, consult a doctor.
Do not get into eye. If contact occurs, rinse thoroughly with water.
Dosage & Administration
Directions - Apply to hands until thoroughly wet - Rub
vigorously until dry.
Package Label.Principal Display Panel
Copy Of Label (Bubble Gum)
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