GOOD NEIGHBOR PHARMACY DIAPER RASH- zinc oxide cream

Good Neighbor Pharmacy Diaper Rash by

Drug Labeling and Warnings

Good Neighbor Pharmacy Diaper Rash by is a Otc medication manufactured, distributed, or labeled by Amerisource Bergen. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                                  Purpose

Zinc oxide 13%.................................................. Skin protectant

PURPOSE

Uses

• helps treat and prevent diaper rash
• protects chafed skin due to diaper rash and helps protect skin from wetness
• helps prevent and temporarily protect chafed, chapped, cracked, or windburned skin and lips

WARNINGS

Warnings

For external use only

DO NOT USE

Do not use over deep or puncture wounds, infections, or lacerations

WHEN USING

When using this product avoid contact with the eyes

ASK DOCTOR

Stop use and ask a doctor if condition worsens or does not improve within 7 days

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Directions

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

STORAGE AND HANDLING

Other information

• Store at 20° to 25°C (68° to 77° F)
• Lot No & Exp Date: see box or see crimp of tube

INACTIVE INGREDIENT

Inactive ingredients aloe vera leaf, dimethicone, fragrance, magnesium sulfate hydrate, methylparaben, microcrystalline wax, mineral oil, petrolatum, propylene glycol, propylparaben, sodium hydroxide, sorbitan sesquioleate, tocopherol acetate, yellow wax, water

DOSAGE & ADMINISTRATION

DISTRIBUTED BY:

Amerisource Bergen

1300 Morris Drive

Chesterbrook, PA 19087

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOOD NEIGHBOR PHARMACY DIAPER RASH 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 46122-279
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	13 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIMETHICONE (UNII: 92RU3N3Y1O)
METHYLPARABEN (UNII: A2I8C7HI9T)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
MINERAL OIL (UNII: T5L8T28FGP)
PETROLATUM (UNII: 4T6H12BN9U)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
YELLOW WAX (UNII: 2ZA36H0S2V)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 46122-279-46	1 in 1 CARTON	10/06/2016
1		57 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	09/23/2014

Labeler - Amerisource Bergen (007914906)