FDA Label for Suave Powder Roll On Antiperspirant And Deodorant
View Indications, Usage & Precautions
Suave Powder Roll On Antiperspirant And Deodorant Product Label
The following document was submitted to the FDA by the labeler of this product Conopco Inc. D/b/a Unilever. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active Ingredient
Aluminum Chlorohydrate (22%)
Otc - Purpose
Purposeanti-perspirant
Indications & Usage
Usesreduces underarm wetness24 hour protection
Warnings
WarningsFor 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 rash or 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
Dosage & Administration
Directions apply to underarms only
Inactive Ingredient
Inactive ingredientsWater (Aqua)PPG-11 Stearyl EtherSteareth-2Steareth-20Fragrance (Parfum)Glycerin
Otc - Questions
Questions? Call 1-800-782-8301
Package Label.Principal Display Panel
2.7 fl oz PDP
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