Buttiezzz Daily

Manufacturer
Fortunique B.V.
Effective date
2016-12-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:48:12

Label at a glance#

ProductButtiezzz Daily
Active ingredientZINC OXIDE
Label structure10 sections

Indications and uses

Helps treat and prevent diaper rash Helps seal out wetness

Dosage and administration

Change wet or soiled diapers promptly Shake well before use Make sure the skin is clean and dry before use.Use a sweeping movement to spray-on the cream in a thin and uniform layer on the buttocks Allow to dry Use a spraying distance approximately 2 to 3 inches Apply Buttiezzz Daily liberally as often as necessary or at every diaper change

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 4%

Purpose

DOSAGE & ADMINISTRATION SECTION

Skin protectant

Uses

OTC - PURPOSE SECTION

Helps treat and prevent diaper rash

Helps seal out wetness

Warning

WARNINGS SECTION

For external use only

When using this product

Avoid contact with eyes

Stop use and contact a Doctor if:

OTC - STOP USE SECTION

Condition worsens

Symptoms last more than 7 days or clear up and occur again within a few days

Not to be applied over deep or puncture wound, infection or lacerations

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

INDICATIONS & USAGE SECTION

Change wet or soiled diapers promptly

Shake well before use

Make sure the skin is clean and dry before use.Use a sweeping movement to spray-on the cream in a thin and uniform layer on the buttocks

Allow to dry

Use a spraying distance approximately 2 to 3 inches

Apply Buttiezzz Daily liberally as often as necessary or at every diaper change

Other information

INSTRUCTIONS FOR USE SECTION

Store at room temperature below 77º F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua)

Coco-Caprylate/Caprate

Glycerin

Alkyl- Alcohols

Alkyl Glucoside

Propylene glycol

Cocoglycerides

Caprylyl Glycol

Capryl-Hidroxamic acid

Chamomilla Recutita(Matricaria)Flower Extract

Calendula Officinalis Flower Extract

Silica

Oleic Acid

Principle Display Panel.50ml Bottle Spray carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Butiezzz Daily CartonButiezzz Daily Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1733707zinc oxide 4 % Topical SprayPSN2
1733707zinc oxide 40 MG/ML Topical SpraySCD2
1733707zinc oxide 4 % Topical SpraySY2
1733707ZNO 40 MG/ML Topical SpraySY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70359-4101-12020-01-31C16284748780-19d75b9d1-1f74-f424-e053-dadaa90a57ce29b8e3ae-3006-3a96-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70359-4101-1Buttiezzz Daily50 g in 1 BOTTLE, SPRAYSPRAY502
70359-4101-1Buttiezzz Daily1 in 1 CARTONSPRAY12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70359-4101BUTTIEZZZ DAILY (ZINC OXIDE) SPRAY [FORTUNIQUE B.V.]2Legacy NDC, 2 package rows20161217_29b8e3ae-3006-3a96-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70359-410170359-4101-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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
43a42dcc-1c9f-3881-e054-00144ff8d46c29b8e3ae-3006-3a96-e054-00144ff8d46c2016-12-14WarningsExact identifier
spl id: 43a42dcc-1c9f-3881-e054-00144ff8d46c
spl set id: 29b8e3ae-3006-3a96-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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