Active Ingredient
Pyrithione Zinc 1%
Blade Howl
FDA Label NDC 59779-422
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cvs Pharmacy Inc for the product Blade Howl (NDC 59779-422). 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, uses, warnings, when using this product, stop using this product and ask a doctor if, 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
Antidandruff
Uses
To help prevent recurrence of flaking and itching associated with dandruff
Warnings
For external use only.
When Using This Product
Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop Using This Product And Ask A Doctor If
condition worsens or does not improve after regular use of this product as directed.
Keep Out Of Reach Of Children
In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.
Directions
For maximum dandruff control, use every time you shampoo. Wet hair, massage onto scalp and rinse . Repeat if desired.
Inactive Ingredients
Water (Aqua), Sodium Laureth Sulfate, Acrylates
Copolymer, Polyquaternium-7, Cocamide MEA, Glycol Distearate, Cocamidopropyl
Betaine, Fragrance (Parfum), Dimethicone, Sodium Chloride, Tetrasodium EDTA,
Sodium Hydroxide, Citric Acid DMDM
Hydantoin, Blue 1 (CI 42090), Red 33 (CI 17200).
Package Front And Back Labels
blade.jpg
12 Oz Front And Bakc Labels (Blade)
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