NDC 67777-226 Zinc Oxide

  1. Labeler Index
  2. Dynarex Corporation
  3. NDC: 67777-226 Zinc Oxide

NDC Product Code 67777-226

NDC CODE: 67777-226

Proprietary Name: Zinc Oxide What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
  • This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.

NDC Code Structure

NDC 67777-226-01

Package Description: 144 PACKET in 1 BOX > 5 g in 1 PACKET

NDC 67777-226-02

Package Description: 36 PACKET in 1 BOX > 15 g in 1 PACKET

NDC 67777-226-03

Package Description: 24 TUBE in 1 CASE > 114 g in 1 TUBE

NDC 67777-226-04

Package Description: 427.5 g in 1 JAR

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Zinc Oxide with NDC 67777-226 is a product labeled by Dynarex Corporation. The generic name of Zinc Oxide is . The product's dosage form is and is administered via form.

Labeler Name: Dynarex Corporation

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
  • LANOLIN (UNII: 7EV65EAW6H)
  • CETETH-10 (UNII: LF9X1PN3XJ)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • PARAFFIN (UNII: I9O0E3H2ZE)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLPARABEN SODIUM (UNII: 625NNB0G9N)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • STEARETH-20 (UNII: L0Q8IK9E08)
  • POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
  • POLYSORBATE 60 (UNII: CAL22UVI4M)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • CHOLECALCIFEROL (UNII: 1C6V77QF41)
  • VITAMIN A (UNII: 81G40H8B0T)
  • ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Dynarex Corporation
Labeler Code: 67777
Start Marketing Date: 02-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2019 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Zinc Oxide Product Label Images

Zinc Oxide Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active Ingredient               PurposeZinc Oxide (1.8% w/w)      Skin Protectant

Purpose:

  • Helps treat and prevent diaper rashTemporarily protects minor cutsscrapes andburnsdries the oozing and weeping ofpoison ivypoison oakpoison sumac

Warnings:

For External Use Only.

When Using This Product:

Do not get in eyes.

Stop Use And Ask A Doctor If:

  • Condition worsenssymptoms last more than 7 days or clear up and occur again in a few days, consult a physician

Keep Out Of Reach Of Children.

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

Dosage And Administration:

  • For skin protectant:Apply liberally as needed           For diaper Rash:change wet and soiled diapers promptlyallow to dryapply ointment liberally with each diaper change

Other Information:

  • Store at room temperature avoid excessive heat contains color additives including FDC yellow # 5

Indications & Usage

Indications: For use as a general skin protectant and diaper rash.

Inactive Ingredient

Inactive ingredients:Aloe Vera Leaf, Alpha-Tocopherol, Ceteth-10, Cetostearyl Alcohol, Cetyl Alcohol, Cholecalciferol, Glycerin, Lanolin, Lavender, Methylparaben, Mineral Oil, Paraffin, Petrolatum, Phenoxyethanol, Polyethylene Glycol 6000, Polysorbate 60, Propylparaben Sodium, Steareth-20, Trolamine, Vitamin A, Water

* Please review the disclaimer below.