FDA.reportPublic FDA data

Gillette ® Hydra Gel Vitamin E

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2020-02-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:03:36

Label at a glance#

ProductGillette Hydra Vitamin E
Active ingredientALUMINUM ZIRCONIUM OCTACHLOROHYDREX 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 octachlorohydrex Gly 16% (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

Water, cyclopentasiloxane, dimethicone, propylene glycol, calcium chloride, PEG/PPG-18/18 dimethicone, fragrance, tocopherol (vitamin E)

Questions?

OTC - QUESTIONS SECTION

1-800-445-5388

SPL UNCLASSIFIED SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gillette ®

HYDRA GEL

48 HOUR PROTECTION

DERMATOLOGIST-TESTED

VITAMIN E

ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
ANTI-PERSPIRANT/DEODORANT

NET WT. 3.8 OZ (107 g)

GilletteGillette

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69423-272-102022-01-28C16284748780-19d75b9d0-7e19-f424-e053-dadaa90a57ceGillette ® Hydra Gel Vitamin E
69423-272-102020-02-03C16284748780-19d75b9d0-7e19-f424-e053-dadaa90a57ceGillette ® Hydra Gel Vitamin E
69423-272-102020-01-31C16284748780-19d75b9d0-7e19-f424-e053-dadaa90a57ceGillette ® Hydra Gel Vitamin E

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69423-272-10Gillette Hydra Vitamin E107 g in 1 CYLINDERGEL1072

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69423-272GILLETTE HYDRA VITAMIN E (ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY) GEL [THE PROCTER & GAMBLE MANUFACTURING COMPANY]2Legacy NDC, 1 package rows20200204_6bc82276-1903-6830-e053-2991aa0a59e0.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-27269423-272-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
TOCOPHEROLR0ZB2556P8IACT
CYCLOMETHICONE 50THT5PCI0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DIMETHICONE92RU3N3Y1OIACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLYP9D3YP29MYACTIB

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
9db30229-3032-ff10-e053-2995a90aff756bc82276-1903-6830-e053-2991aa0a59e02020-02-03WarningsExact identifier
spl id: 9db30229-3032-ff10-e053-2995a90aff75
spl set id: 6bc82276-1903-6830-e053-2991aa0a59e0

Reported adverse events (FAERS/openFDA)#

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