FDA.reportPublic FDA data

Helmm Antiperspirant Deodorant Coastline

Manufacturer
ZGTL, LLC | Raining Rose
Effective date
2026-02-04
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:37:00

Label at a glance#

ProductHelmm Antiperspirant Deodorant Coastline
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydren GLY (18%)

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Cetyl Alcohol, C12-C15 Alkyl Benzoate, Dimethicone 10 CST, Hydrogenated Castor Oil, Behenyl Alcohol, Sunflower Seed Oil, Vegetable Glycerin, Tapioca Starch, Steareth-2, Corn Starch, Fragrance, Vitamin E Acetate, Aloe Leaf Extract

INDICATIONS & USAGE SECTION

Uses: reduces underarm wetness

WARNINGS SECTION

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

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.

DOSAGE & ADMINISTRATION SECTION

  • Apply to underarms only.
  • Twist dial knob use product.
  • To remove cartridge, squeeze tabs and pull.
  • To insert cartridge, align tabs and press down.

OTC - PURPOSE SECTION

Uses: reduces underarm wetness​

RECENT MAJOR CHANGES SECTION

  • Apply to underarms only.
  • Twist dial knob use product.
  • To remove cartridge, squeeze tabs and pull.
  • To insert cartridge, align tabs and press down.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Coastline Antiperspirant & Deodorant LabelCoastline Antiperspirant & Deodorant Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72147-1804-12025-02-18C16284748780-11030e365-6b47-111a-e063-dadaa90a10e2Helmm Antiperspirant and Deodorant - Coastline
72147-1804-12024-01-30C16284748780-11030e365-6b47-111a-e063-dadaa90a10e2Helmm Antiperspirant and Deodorant - Coastline

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72147-1804-1Helmm Antiperspirant Deodorant Coastline71 g in 1 TUBE, WITH APPLICATORGEL714

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72147-180472147-1804-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
STARCH, CORNO8232NY3SJIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
STARCH, TAPIOCA24SC3U704IIACT
STEARETH-2V56DFE46J5IACT
CYCLOMETHICONE 50THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
C12-15 ALKYL ETHYLHEXANOATEGQJ580CH83IACT
DOCOSANOL9G1OE216XYIACT
SUNFLOWER OIL3W1JG795YIIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
CETYL ALCOHOL936JST6JCNIACT
DIMETHICONE 20H8YMB5QY0DIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT

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
Helmm Antiperspirant Deodorant CoastlineALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLYZGTL, LLCb6c37efa-cbf5-db3d-e053-2995a90aa46a2026-02-04WarningsExact identifier
ndc (package): 72147-1804-1
ndc (product): 72147-1804
ndc11 (package): 72147180401
spl id: 4a02ecc7-8c1f-91d9-e063-6394a90a98fb
spl set id: b6c37efa-cbf5-db3d-e053-2995a90aa46a

Reported adverse events (FAERS/openFDA)#

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