Active Ingredient
SELENIUM SULFIDE 1% (ANTI DANDRUFF)
Antidandruff
FDA Label NDC 21130-610
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Safeway Inc for the product Antidandruff (NDC 21130-610). 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, uses and directions, warnings, ask a doctor before using if you have, when using this product, stop use and ask a doctor if, keep out of reach of children, package front and back labels, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses And Directions
- USES: FOR RELIEF OF FLAKING AND ITCHING DUE TO DANDRUFF, AND SEBORRHEIC DERMATITIS, AND TO HELP PREVENT THE CHANCE OF RE-OCCURRENCE.
- DIRECTIONS:SHAKE WELL, SHAMPOO, THEN RINSE THOROUGHLY. FOR BEST RESULTS, USE AT LEAST TWICE A WEEK OR AS DIRECTED BY A DOCTOR.
Warnings
- FOR EXTERNAL USE ONLY.
Ask A Doctor Before Using If You Have
SEBORRHEIC DERMATITIS IN AREAS OTHER THAN THE SCALP
When Using This Product
- AVOID CONTACT WITH THE EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER. FOR USE ON COLOR-TREATED OR PERMED HAIR, RINSE THOROUGHLY.
Stop Use 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
- IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
Package Front And Back Labels
11OZ FRONT AND BACK LABELS: safeway11.jpg
11 Oz Front And Back Labels (Safeway11)
Questions/Comments?
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