NDC 71611-010 Epsom Salt Baby Beauty

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71611-010
Proprietary Name:
Epsom Salt Baby Beauty
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Click Products Llc
Labeler Code:
71611
Start Marketing Date: [9]
10-19-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 71611-010-01

Package Description: 454 g in 1 BAG

NDC Code 71611-010-02

Package Description: 907 g in 1 BOX

NDC Code 71611-010-03

Package Description: 1361 g in 1 BAG

NDC Code 71611-010-04

Package Description: 1814 g in 1 BAG

Product Details

What is NDC 71611-010?

The NDC code 71611-010 is assigned by the FDA to the product Epsom Salt Baby Beauty which is product labeled by Click Products Llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 71611-010-01 454 g in 1 bag , 71611-010-02 907 g in 1 box , 71611-010-03 1361 g in 1 bag , 71611-010-04 1814 g in 1 bag . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Epsom Salt Baby Beauty?

USESInternal Relieves occasional constipation (irregularity)Generally produces bowel movements in 1/2 to 6 hoursExternal - RElieves pain from minor prains and bruises

Which are Epsom Salt Baby Beauty UNII Codes?

The UNII codes for the active ingredients in this product are:

  • MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
  • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)

What is the NDC to RxNorm Crosswalk for Epsom Salt Baby Beauty?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[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".