Secret Clinical Strength Odor Shield with Charcoal Invisible

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2023-03-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:34:59

Label at a glance#

ProductSecret Clinical Strength Odor Shield with Charcoal Invisible
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure10 sections

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum zirconium tetrachlorohydrex Gly 20% (anhydrous)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

  • reduces underarm wetness

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

OTC - STOP USE SECTION

Stop use if rash or irritation occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply to underarms only.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, stearyl alcohol, mineral oil, PPG-14 butyl ether, cyclodextrin, petrolatum, hydrogenated castor oil, talc, fragrance, C20-40 pareth-10, dimethicone, corn starch/maltodextrin crosspolymer, behenyl alcohol, panthenyl triacetate, charcoal powder

Questions?

OTC - QUESTIONS SECTION

1-800-964-1947

SPL UNCLASSIFIED SECTION

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202.

PRINCIPAL DISPLAY PANEL - 45 g Cylinder Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Secret®

CLINICAL
STRENGTH ®

ODOR SHIELD

WITH CHARCOAL

Invisible Solid With Charcoal

ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
ANTIPERSPIRANT/DEODORANT

NET WT. 1.6 OZ (45 g)

Secret1Secret1

FDA-Initiated Inactive NDC Indexing#

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-39969423-399-45

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f6564bf0-705e-639a-e053-2a95a90afe71a2663521-bedc-af9f-e053-2995a90a76a62023-03-07WarningsExact identifier
spl id: f6564bf0-705e-639a-e053-2a95a90afe71
spl set id: a2663521-bedc-af9f-e053-2995a90a76a6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.