NDC 76271-001 Dr. Waltons Baby Powder
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76271 - Dr. Waltons, Incorporated
- 76271-001 - Dr. Waltons
Product Packages
NDC Code 76271-001-02
Package Description: 55 g in 1 BOTTLE, PLASTIC
NDC Code 76271-001-24
Package Description: 675 g in 1 BOTTLE, PLASTIC
Product Details
What is NDC 76271-001?
What are the uses for Dr. Waltons Baby Powder?
Which are Dr. Waltons Baby Powder UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Dr. Waltons Baby Powder 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:
- TALC (UNII: 7SEV7J4R1U)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[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".