RITE AID DIAPER RASH- zinc oxide ointment

Rite Aid Diaper Rash by

Drug Labeling and Warnings

Rite Aid Diaper Rash by is a Otc medication manufactured, distributed, or labeled by RiteAid Corporation, Pharma Pac, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                            Purpose

Zinc Oxide. 40%.......................................Skin protectant

PURPOSE

Uses

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

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.
If swallowed, get medical help or contact
a Poison Control Center right away.

INDICATIONS & USAGE

Uses

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

WARNINGS

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 the reach of children. If swallowed get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION

Directions

- change wet and soiled diapers promptly
- cleanse the diaper area
- allow to dry
- apply ointment liberally as often as necessary, with each diaper change,
especially at bedtime or anytime when exposure to wet diapers may be prolonged

Other information

Store at 20 degrees to 25 degrees C (68 degrees to 77 degrees F)

INACTIVE INGREDIENT

Inactive Ingredients

BHA, cod liver oil, fragrance, lanolin, methylparaben, petrolatum, purified water, talc

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

RITE AID DIAPER RASH 
zinc oxide ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11822-0376
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	400 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)
LANOLIN (UNII: 7EV65EAW6H)
METHYLPARABEN (UNII: A2I8C7HI9T)
BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
WATER (UNII: 059QF0KO0R)
TALC (UNII: 7SEV7J4R1U)
COD LIVER OIL (UNII: BBL281NWFG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11822-0376-3	1 in 1 CARTON
1		113 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	07/20/2010

Labeler - RiteAid Corporation (014578892)

Registrant - Pharma Pac, LLC (140807475)

Establishment
Name	Address	ID/FEI	Business Operations
Pharma Pac, LLC		140807475	manufacture