Biosilk
FDA Label NDC 73740-5050
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Farouk Systems, Inc. for the product Biosilk (NDC 73740-5050). 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, inactive ingredients, keep out of reach of children, purpose, uses, warnings, directions, primary display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredients
Inactive ingredients: Aqua/Water/Eau, Dimethicone,
Cetyl Alcohol, C15-19 Alkane, Propanediol, Glycerin, Cetearyl
Alcohol, Glyceryl Stearate SE, Ceteareth-20, Caprylyl Glycol,
Aloe Barbadensis Leaf Juice, Lavandula Angustifolia
(Lavender) Oil, Hydrolyzed Silk, Dimethiconol, Hexylene
Glycol, Butyrospermum Parkii (Shea) Butter, Pentylene
Glycol, Ethylhexylglycerin, Dicetyldimonium Chloride, Alcohol
Denat., Sodium Hydroxide, Fragrance (Parfum), Benzyl
Benzoate, Butylphenyl Methylpropional, Coumarin, Linalool
Keep Out Of Reach Of Children
Purpose
Uses
Warnings
Warnings
For external use only.
When using this product
avoid contact with eyes
if contact occurs, rinse eyes thoroughly with water
Stop use and ask a doctor if irritation and redness develop
Keep out of reach of children. In case of accidental ingestion,
get medical help or contact a Poison Control Center immediately.
Directions
Primary Display Panel
* Please review the disclaimer below.