FDA.reportPublic FDA data

5 Day

Manufacturer
NUMARK BRANDS, INC | Span Packaging Services LLC
Effective date
2016-07-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:24:59

Label at a glance#

Product5 Day
Active ingredientAluminum Zirconium Tetrachlorohydrex Gly
Label structure12 sections

Dosage and administration

apply to underarms only tilt bottle roll on to cover entire underarm area use daily after bathing replace cap tightly

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientPurpose
Aluminum zirconium tetrachlorohydrex glycine 20%Antiperspirant

INDICATIONS & USAGE SECTION

Uses  reduces underarm perspiration

Warnings

WARNINGS SECTION

For external use only

OTC - ASK DOCTOR SECTION

Consult 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
  • immediately after bathing

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

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
  • tilt bottle
  • roll on to cover entire underarm area
  • use daily after bathing
  • replace cap tightly

Inactive ingredients

INACTIVE INGREDIENT SECTION

fragrance, glycerin, glyceryl stearate, lauryl lactate, magnesium aluminum silicate, PEG 100 stearate, Polysorbate 20, triclosan, water 

Questions?

OTC - QUESTIONS SECTION

Call 1-800-331-0221

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

Dist. by: NUMARK LABORATORIES INC.
EDISON, NJ 08818    Rev. 7/11   C-12060

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ROLL-ON
REGULAR SCENT
ANTIPERSPIRANT & DEODORANT
 
5 DAY®

2.5 FL OZ (74 ml)

Dist. by: NUMARK LABORATORIES INC.
EDISON, NJ 08818    Rev. 7/11   C-12060

Label
Label

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69846-02069846-020-22

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
Aluminum Zirconium Tetrachlorohydrex Gly8O386558JEACTIB
GlycerinPDC6A3C0OXIACT
Glyceryl Monostearate230OU9XXE4IACT
Lauryl LactateG5SU0BFK7OIACT
Magnesium Aluminum Silicate6M3P64V0NCIACT
Peg-100 StearateYD01N1999RIACT
Polysorbate 207T1F30V5YHIACT
Triclosan4NM5039Y5XIACT
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
53de5d5b-ea17-4010-996f-6a21e1df8178f6b49e9f-56e4-6950-be20-a1ff41c0a9e92020-12-11WarningsExact identifier
spl set id: f6b49e9f-56e4-6950-be20-a1ff41c0a9e9

Reported adverse events (FAERS/openFDA)#

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