BAMBOOBIES DIAPER RASH- zinc oxide 15% spray

Bamboobies Diaper Rash by

Drug Labeling and Warnings

Bamboobies Diaper Rash by is a Otc medication manufactured, distributed, or labeled by Derma Care Research Labs, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide 15%

PURPOSE

Skin Protectant

INDICATIONS & USAGE

Helps treat and prevent diaper rash, protects chafed skin due to diaper rash.

WARNINGS

For external use only.

When using this product do not get into eyes.

Stop use and ask a doctor if condition worsens, symptoms last more than 7 days or clear up and occur again within a few days.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Change wet and soiled diapers promptly. Cleanse the diaper area. Allow to dry. Shake well before each use. Spray liberally onto affected area with each diaper change, especially at bedtime or anytime when exposure to wet diaper may be prolonged. Apply as needed.

INACTIVE INGREDIENT

Aloe Barbadensis Leaf Juice, Bentonite, Butyrospermum Parkii (Shea) Butter, Calendula Officinalis flower Extract, Caprylhydroxamic Acid, Caprylyl Glycol, Cellulose Gum, Cetearyl Alcohol, chamomilla Recutita (Matricaria) Flower Extract, Coco-Glucoside, Glycerin, Glyceryl Oleate, Glyceryl Rosinate, Helianthus Annuus (Sunflower) Seed Oil, Microcrystalline Cellulose, Olea Europaea (Olive) Fruit Oil, Olea Europaes 9Olive) Oil Unsaponifiables, Propanediol, Ricinus Communis (Castor) Seed Oil, Water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BAMBOOBIES DIAPER RASH 
zinc oxide 15% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72839-132
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	15 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SHEA BUTTER (UNII: K49155WL9Y)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL OLEATE (UNII: 4PC054V79P)
OLEA EUROPAEA (OLIVE) OIL UNSAPONIFIABLES (UNII: XO45V955LT)
PROPANEDIOL (UNII: 5965N8W85T)
BENTONITE (UNII: A3N5ZCN45C)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
GLYCERYL ROSINATE (UNII: SD112V492J)
OLIVE OIL (UNII: 6UYK2W1W1E)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
COCO GLUCOSIDE (UNII: ICS790225B)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CHAMOMILE (UNII: FGL3685T2X)
SUNFLOWER OIL (UNII: 3W1JG795YI)
CASTOR OIL (UNII: D5340Y2I9G)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72839-132-03	100.5 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	03/09/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	M016	03/09/2023

Labeler - Derma Care Research Labs, LLC (116817470)

Registrant - Derma Care Research Labs, LLC (116817470)

Establishment
Name	Address	ID/FEI	Business Operations
Derma Care Research Labs, LLC		116817470	manufacture(72839-132)