Otc - Active Ingredient
CHLOROXYLENOL............1%
Softcide
FDA Label NDC 71695-200
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Vwr International for the product Softcide (NDC 71695-200). 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 - keep out of reach of children, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
ANTICEPTIVE AGENT
Indications & Usage
Handwash to help reduce bacteria that can potentially cause disease. Reduces the risk and chance of cross -infection.
Warnings
For external use only.
If swallowed seek medical help or contact poison control immediately
Avoid contact with eyes. If contact occurs flush with water
Discontinue use and contact a health practitioner if irritation develops
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN
Dosage & Administration
Wet skin and apply a sufficient amount on hands and forearms
Scrub well and rinse thoroughly after washing
Inactive Ingredient
OLIVE OIL
WALNUT OIL
JOJOBA OIL
RICE BRAN OIL
GAMOLENIC ACID
ALKYL (C12-15) BENZOATE
QUATERNIUM-15
EDETATE SODIUM
CITRIC ACID MONOHYDRATE
ALOE VERA LEAF
POLYQUATERNIUM-10 (30000 MPA.S AT 2%)
ALLANTOIN
COCAMIDOPROPYL BETAINE
SODIUM LAURETH SULFATE
COCAMIDOPROPYL HYDROXYSULTAINE
POLYSORBATE 20
PEG-150 DISTEARATE
SODIUM LAUROYL SARCOSINATE
* Please review the disclaimer below.
