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Drug Facts
Manufactured for
Crawford Supply • St. Louis, MO 63132
PRODUCT OF CANADA
Crawford Dandruff
FDA Label NDC 50157-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Brands International for the product Crawford Dandruff (NDC 50157-009). 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 other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, 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
Pyrithione zinc 0.5%
Otc - Purpose
Purpose
Anti dandruff
Indications & Usage
Uses
helps prevent recurrence of flaking and itching associated with dandruff.
Warnings
Warnings using this product
For external use only.
Otc - Keep Out Of Reach Of Children
Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Directions: For maximum dandruff control, use at least twice a week. Wet hair, massage through hair and scalp, rinse and repeat if desired.
Inactive Ingredient
INACTIVE INGREDIENTS:
Water (Aqua), Sodium Laureth Sulfate, Sodium Chloride, Glycol Distearate, Cocamidopropyl Betaine, Polyquaternium-7, Fragrance, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Blue #1
Package Label.Principal Display Panel
Crawford
Dandruff Shampoo
Clears Hair of Dandruff Flakes
4 fl. oz. (118 mL)
* Please review the disclaimer below.
