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Drug Facts
DISTRIBUTED BY:
FAMILY DOLLAR SERVICES, INC.
10401 MONROE RD
MATTHEWS, NC 28105 USA
Family Dollar Roll-on Deodorant
FDA Label NDC 55319-240
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Family Dollar Services,inc. for the product Family Dollar Roll-on Deodorant (NDC 55319-240). 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, active ingredients, purpose, uses, warnings, otc - do not use, otc - ask doctor, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Aluminum Chlorohydrate 16 % ( Anhydrous)
Purpose
Antiperspirant
Uses
Reduces underarm wetness
Warnings
For external use only.
Otc - Do Not Use
Do not use on broken skin
Otc - Ask Doctor
Ask a doctor before use if you have kidney disease.
Otc - Stop Use
Stop use if irritation occurs.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply to underarms only
Inactive Ingredients
Water
Steareth-2
Steareth-20
PPG-15 Stearyl Ether
Mineral Oil
Magnesium Aluminum Silicate
Fragrance
Disodium EDTA
BHT
Principal Display Panel - 50.2 Ml Bottle Label
FAMILY
DOLLAR®
100% SATISFACTION
OR YOUR MONEY BACK
GUARANTEED
compare to
TUSSY®*
Roll-On
Deodorant
1.7 FL OZ (50.2mL)
Principal Display Panel (50.2 mL Bottle Label)
* Please review the disclaimer below.
