SWEET CHEEKS DIAPER SPRAYER- zinc oxide diaper paste spray spray

Sweet Cheeks Diaper Sprayer by

Drug Labeling and Warnings

Sweet Cheeks Diaper Sprayer by is a Otc medication manufactured, distributed, or labeled by Tubby Todd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Zinc Oxide 14.9%

Purpose

Skin protectant

Uses

helps treat and prevent diaper rash
protects chafed skin due to diaper rash and helps seal out wetness

Warnings

For external use only.

When using this product

do not use near eyes. In case of contact, rinse eyes thoroughly with water.

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 immediately

Directions

shake well before use
change wet or soiled diapers promptly
cleanse the diaper area and allow to dry
spray 4-6 inches away from skin
apply with each diaper change and as often as necessary
turn clip to lock position when not in use.

Other information

store at room temperature
may stain some fabrics

Inactive ingredients

Inactive ingredients

Aloe Barbadensis Leaf Juice, Bentonite, Butyrospermum Parkii (Shea) Butter, Calendula Officinalis Flower Extract, Caprylhydroxamic Acid, Caprylyl Glycol, Cellulose Gum, Cetearyl Alcohol, Coco-Glucoside, Glycerin, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Microcrystalline Cellulose, Olea Europaea (Olive) Fruit Oil, Propanediol, Ricinus Communis (Castor) Seed Oil, Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SWEET CHEEKS DIAPER SPRAYER 
zinc oxide diaper paste spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73088-304
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	14.9 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BENTONITE (UNII: A3N5ZCN45C)
CELLULOSE GUM (UNII: K679OBS311)
GLYCERIN (UNII: PDC6A3C0OX)
OLEA EUROPAEA (OLIVE) FRUIT OIL (UNII: 6UYK2W1W1E)
RICINUS COMMUNIS (CASTOR) SEED OIL (UNII: D5340Y2I9G)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
COCO-GLUCOSIDE (UNII: ICS790225B)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
PROPANEDIOL (UNII: 5965N8W85T)
WATER (UNII: 059QF0KO0R)
HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)
ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73088-304-04	85 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	10/01/2024

Labeler - Tubby Todd (052545299)