ZINC OXIDE - zinc oxide ointment 
RiteAid

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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drug facts


Active ingredient                      Purpose


Zinc Oxide........................................Skin protectant


Active ingredient                 Purpose

Zinc Oxide.................................Skin protectant

Uses

- dries the oozing and weeping od poison - ivy - oak - sumac
- helps treat and prevent diaper rash
- protects chafed skin associated with diaper rash and helps protect from wetness


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


Uses

- dries the oozing and weeping od poison - ivy - oak - sumac
- helps treat and prevent diaper rash
- protects chafed skin associated with diaper rash and helps protect from wetness

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


Directions

- apply as needed

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

- children under 12 years

ask a doctor

Other information

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


Inactive Ingredients

beeswax, mineral oil, petrolatum

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ZINC OXIDE 
zinc oxide ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0081
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE200 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
WHITE WAX (UNII: 7G1J5DA97F)  
LIGHT MINERAL OIL (UNII: N6K5787QVP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11822-0081-357 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34705/19/2009
Labeler - RiteAid (014578892)
Registrant - Pharma Pac, LLC (140807475)
Establishment
NameAddressID/FEIBusiness Operations
Pharma Pac, LLC140807475manufacture

Revised: 2/2011
Document Id: 0a9bbc5a-bc61-439e-b7ea-35247478e10c
Set id: 8a3421c6-8533-4e93-b31d-f497fe33c80b
Version: 2
Effective Time: 20110216
 
RiteAid