FDA.reportPublic FDA data

5 Day

Manufacturer
NUMARK BRANDS, INC
Effective date
2025-12-15
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
full-release
Hydrated at
2026-06-01 01:26:25

Label at a glance#

Product5 Day
Active ingredientAluminum Chlorohydrate
Label structure12 sections

Dosage and administration

apply to underarms only use daily after bathing store upright

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientPurpose
Aluminum chlorohydrate 25%Antiperspirant

INDICATIONS & USAGE SECTION

Uses  reduces underarm perspiration

Warnings

WARNINGS SECTION

For external use only

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

Do not use

OTC - DO NOT USE SECTION

  • immediately after shaving
  • on broken skin
  • on irritated skin

When using this product

OTC - WHEN USING SECTION

  • do not use in or near eyes
  • apply to underarms only

OTC - STOP USE SECTION

Stop use and ask a doctor if rash or irritation develops

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
  • use daily after bathing
  • store upright

INACTIVE INGREDIENT SECTION

Inactive ingredients alcohol, benzethonium chloride, fragrance, octoxynol-9, water

OTC - QUESTIONS SECTION

Questions? Call 1-800-214-2379

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REGULAR SCENT

FRESH EVERY TIME® 

Single Use Pads

5 DAY®

75 Antiperspirant & Deodorant Pads

If you have any questions or difficulties
finding this product, please go to
our website: www.numarkbrands.com

Distributed by: Numark Brands, Inc.
Edison, NJ 08818    1-800-214-2379
D12088     Rev 10/18

Label
Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130038485110426GTIN-13: 0038485110426
EAN-13: 0038485110426
GTIN-12: 038485110426
UPC-A: 038485110426
GTIN storage (14 digits): 00038485110426		5day75pads.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69846-110-425 Day75 in 1 JARLIQUID7510

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69846-11069846-110-42

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
Aluminum ChlorohydrateHPN8MZW13MACTIB
Alcohol3K9958V90MIACT
Benzethonium ChloridePH41D05744IACT
Water059QF0KO0RIACT

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
5 DayALUMINUM CHLOROHYDRATENUMARK BRANDS, INC571ca761-9696-7316-963d-c899897efa422025-12-15WarningsExact identifier
ndc (package): 69846-110-42
ndc (product): 69846-110
ndc11 (package): 69846011042
spl id: 465b997b-aa0a-423e-aa3c-8eb58422d51d
spl set id: 571ca761-9696-7316-963d-c899897efa42

Reported adverse events (FAERS/openFDA)#

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