FDA Label for Ainnara Roll-on
View Indications, Usage & Precautions
Ainnara Roll-on Product Label
The following document was submitted to the FDA by the labeler of this product Ventura Corporation Ltd.. 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.
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Drug Facts
Dist. by Ventura Corporation LTD., San Juan, Puerto Rico, 00926
Active Ingredients
Aluminum sesquichlorohydrate (17%)
Purpose
Antiperspirant
Uses
- reduces underarm wetness.
Warnings
- For external use only.
Otc - Do Not Use
- Do not use on broken skin.
Otc - Stop Use
- Stop use and ask a doctor if rash and irritation occurs.
Otc - Ask Doctor
- Ask a doctor before use if you have kidney disease.
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
Aqua (water), steareth-2, ppg-15 stearyl ether, steareth-21, dicaprylyl carbonate, fragrance, cyclopentasiloxane, triclosan, cyclohexasiloxane, benzalkonium chloride, tetrasodium edta, methylparaben, bisabolol.
Principal Display Panel - 50 Ml Bottle Label
AÏNNARA
ANTIPERSPIRANT
ROLL-ON DEODORANT
does not contain alcohol
ēsika
50 ml e (1.7 fl.oz.)
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