Active Ingredients
Zinc Oxide 4%
Buttiezzz Daily
FDA Label NDC 70359-4101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Fortunique B.v. for the product Buttiezzz Daily (NDC 70359-4101). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warning, stop use and contact a doctor if:, keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Skin protectant
Uses
Helps treat and prevent diaper rash
Helps seal out wetness
Warning
For external use only
When using this product
Avoid contact with eyes
Stop Use And Contact A Doctor If:
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
If swallowed, get medical help or contact a Poison Control Center right away
Directions
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
Store at room temperature below 77° F
Inactive Ingredients
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
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