FDA.reportPublic FDA data

Cremo Company

Manufacturer
Cremo Company | Raining Rose
Effective date
2025-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:30:10

Label at a glance#

ProductCremo Company
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure8 sections

Dosage and administration

• Apply to underarms only. • Twist up product, apply a light layer to clean and dry underarms

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex GLY (Anhydrous) (20.0%)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on broken skin.

Stop use if

OTC - STOP USE SECTION

skin rash or irritation occurs.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

kidney disease.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply to underarms only. • Twist up product, apply a light layer to clean and dry underarms

Inactive ingredients

INACTIVE INGREDIENT SECTION

Isopropyl Palmitate, C12-15 Alkyl Benzoate, Dimethicone, Hydrogenated Castor Oil, Stearyl Alcohol, PPG-14 Butyl Ether, Glycine, Cetyl Alcohol, Tapioca Starch, Behenyl Alcohol, Helianthus Annuus (Sunflower) Seed Oil, Fragrance, Zea Mays (Corn) Starch, Water, Steareth-2, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Polycitronellol

Questions

OTC - QUESTIONS SECTION

Call toll-free 800-853-1762

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDPPDPCremo
BOURBON VANILLA
SMOOTH & CREAMY
WITH SCENT NOTES OF
DISTILLER'S SPICE| AGED OAK | MADAGASCAR VANILLA
Antiperspirant & Deodorant
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
NET WT. 2.65 OZ (75 g)

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71825-121-72Cremo Company75 mL in 1 TUBESTICK751

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71825-12171825-121-72

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
STEARETH-2V56DFE46J5IACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
WATER059QF0KO0RIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
BEHENYL ALCOHOL9G1OE216XYIACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
GLYCINETE7660XO1CIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
DIMETHICONE92RU3N3Y1OIACT
STEARYL ALCOHOL2KR89I4H1YIACT
TAPIOCA STARCH24SC3U704IIACT
ZEA MAYS (CORN) STARCHO8232NY3SJIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
CETYL ALCOHOL936JST6JCNIACT

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
Cremo CompanyALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (ANHYDROUS)Cremo Company471ceea8-e8d5-9a54-e063-6394a90ae86c2025-01-01WarningsExact identifier
ndc (package): 71825-121-72
ndc (product): 71825-121
ndc11 (package): 71825012172
spl id: 471ceea8-e8d6-9a54-e063-6394a90ae86c
spl set id: 471ceea8-e8d5-9a54-e063-6394a90ae86c

Reported adverse events (FAERS/openFDA)#

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