NDC 69968-0713 Johnsons Baby Care Essentials Gift Set
Zinc Oxide Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69968 - Johnson & Johnson Consumer Inc.
- 69968-0713 - Johnsons Baby Care Essentials Gift Set
Product Packages
NDC Code 69968-0713-9
Package Description: 1 KIT in 1 PACKAGE * 100 mL in 1 BOTTLE * 100 mL in 1 BOTTLE * 1 TUBE in 1 CARTON (69968-0061-1) / 28 g in 1 TUBE
Product Details
What is NDC 69968-0713?
What are the uses for Johnsons Baby Care Essentials Gift Set?
Which are Johnsons Baby Care Essentials Gift Set UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Johnsons Baby Care Essentials Gift Set Inactive Ingredients UNII Codes?
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. The UNII codes for the inactive ingredients in this product are:
- PETROLATUM (UNII: 4T6H12BN9U)
- COD LIVER OIL (UNII: BBL281NWFG)
- LANOLIN (UNII: 7EV65EAW6H)
- TALC (UNII: 7SEV7J4R1U)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Johnsons Baby Care Essentials Gift Set?
- RxCUI: 1094560 - zinc oxide 40 % Topical Paste
- RxCUI: 1094560 - zinc oxide 0.4 MG/MG Paste
- RxCUI: 1094560 - zinc oxide 40 % Paste
- RxCUI: 1094560 - ZNO 0.4 MG/MG Paste
- RxCUI: 1797059 - Desitin 40 % Topical Paste
* Please review the disclaimer below.
[1] 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.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] 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.
[12] 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".