Active Ingredient
Triclosan 0.115%
Antibacterial
FDA Label NDC 68391-141
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bjwc for the product Antibacterial (NDC 68391-141). 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, purpose, warnings, when using this product, stop using this product and ask doctor if, keep out of reach of children, questions/comments?, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
- Antibacterial.
Warnings
For external use only.
When Using This Product
Avoid contact with eyes. If contact occurs, rinse with water.
Stop Using This Product And Ask Doctor If
Irritation or redness develops and lasts.
Keep Out Of Reach Of Children
In case of accidental ingestions, get medical help or contact a Poison Control Center immediately.
Questions/Comments?
1-800-934-1204
Directions
Apply to wet hands, lather and rinse thoroughly.
Uses
To help reduce bacteria on the skin
Inactive Ingredeints
Water (Aqua), Sodium Laureth Sulfate, Lauramide DEA, Cocamidopropyl Betaine, Decyl Glucoside, Polyquaternium-7, Saccharomyces, Hydrolyzed Vegetable Protein, Camellia Sinensis (Green Tea) Leaf Extract, Sodium Bicarbonate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Retinyl Palmitate, Ascorbyl Palmitate, Niacinamide, Tetrasodium EDTA, Sodium Chloride, Fragrance (Parfum), DMDM Hydantoin, Citric Acid, Red 33 (CI 17200), Blue 1 (CI 42090).
Package Front And Back Labels
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1gal Front And Back Labels (Bj1g)
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