Secret AP Roll On Deo Powder Fresh

Manufacturer
Aerobal S.A. De C.V.
Effective date
2010-10-05
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 22:26:35

Label at a glance#

ProductSecret AP Roll On Deo Powder Fresh
Active ingredientAluminum Chlorohydrate
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum chlorohydrate 14% (anhydrous)

INACTIVE INGREDIENT SECTION

water, PPG-15 stearyl ether, steareth-2, steareth-20, fragrance, disodium EDTA, BHT

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only

INDICATIONS & USAGE SECTION

Reduces underarm weatness

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.

WARNINGS SECTION

Stop use if rash or irritation occurs.

For external use only.

Do not use on broken skin.

Asak a doctor before use if you have kidney disease.

OTC - PURPOSE SECTION

Antiperspirant/deoderant 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Roll on, Secret powder fresh.
package image
package image
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61962-4490-12019-10-29C16284748780-1960f7f55-c086-8e05-e053-dbdaa90a074aSecret AP Roll On Deoderant Powder Fresh

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61962-4490-1Secret AP Roll On Deo Powder Fresh65 mL in 1 BOTTLESOLUTION655

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61962-4490SECRET AP ROLL ON DEO POWDER FRESH (ALUMINUM CHLOROHYDRATE) SOLUTION [AEROBAL S.A. DE C.V.]51 package rows20101208_c47173b7-b4db-4fd6-ab4f-481ee76c1a65.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Aluminum ChlorohydrateACTIVE INGREDIENTHPN8MZW13M5
Aluminum CationACTIVE MOIETY3XHB1D032B5
DISODIUM 2,2'-DIHYDROXY-4,4'-DIMETHOXY-5,5'-DISULFOBENZOPHENONEINACTIVE INGREDIENT7925W14T4L5
STEARETH-2INACTIVE INGREDIENTV56DFE46J55
STEARETH-20INACTIVE INGREDIENTL0Q8IK9E085
STEARYL ETHYLHEXANOATEINACTIVE INGREDIENTX8707A22745
waterINACTIVE INGREDIENT059QF0KO0R5

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61962-449061962-4490-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 5 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
STEARETH-2STEARETH-2V56DFE46J5OINTMENT / TOPICAL714 mgExact identifier — unii candidate
4 equally ranked IID candidates
STEARETH-20STEARETH-20L0Q8IK9E08CREAM / TOPICAL4.15 %w/wExact identifier — unii candidate
STEARETH-2STEARETH-2V56DFE46J5CREAM / TOPICAL643 mgExact identifier — unii candidate
4 equally ranked IID candidates
STEARETH-2STEARETH-2V56DFE46J5LOTION / TOPICAL0.4 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
STEARETH-2STEARETH-2V56DFE46J5AEROSOL, FOAM / TOPICAL1.09 %w/wExact identifier — unii candidate
4 equally ranked IID candidates

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
8b7d9138-bb81-4ce4-b31d-039b52e3a6c5c47173b7-b4db-4fd6-ab4f-481ee76c1a652010-10-05WarningsExact identifier
spl id: 8b7d9138-bb81-4ce4-b31d-039b52e3a6c5
spl set id: c47173b7-b4db-4fd6-ab4f-481ee76c1a65

Reported adverse events (FAERS/openFDA)#

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