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Drug Facts
Hecho en Puerto Rico por:
Omega & Delta Co., Inc.
P.O. Box 1831, Carolina, P.R. 00984
Odorono Liquid
FDA Label NDC 51048-201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Omega & Delta Co for the product Odorono (NDC 51048-201). 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, indications & usage, warnings, otc - do not use, otc - stop use, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Aluminum Chlorohydrate 20%
Purpose
Antiperspirant
Indications & Usage
Use: Reduces underarm wetness
Warnings
Warnings: For external use only
Otc - Do Not Use
Do not use on broken skin
Otc - Stop Use
Stop use if rash or 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.
Dosage & Administration
Directions: Apply evenly to underarms only
Inactive Ingredient
Inactive Ingredients: Water, PPG-15 Stearyl Ether, Steareth-2, Steareth-21, Fragrance, Disodium EDTA, BHT, Triclosan
Package Label.Principal Display Panel
* Please review the disclaimer below.
