Risk Seduction
FDA Label NDC 37808-688

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by H-e-b for the product Risk Seduction (NDC 37808-688). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredient

Aluminum Zirconium Trichlorohydrex 17.3% (anhydrous)

Otc - Purpose

Purpose

Antiperspirant

Indications & Usage

Use

Reduces underarm wetness

Warnings

Warnings

For external use only

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use if rash or irritation occurs

Keep out of the reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.


Dosage & Administration

Directions

Turn dial to raise stick, apply to underarms only.

Inactive Ingredient

Inactive Ingredientscyclomethicone, stearyl alcohol, mineral oil, hydrogenated castor oil, diisopropyl adipate, cetyl alcohol, aluminum starch octenylsuccinate, glyceryl stearate (and) PEG-100 stearate, fragrance, PPG-14 butyl ether, silica, talc

Package Label.Principal Display Panel

Image of 76 g Label

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