NDC 75957-003 Boogie Bottoms

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:
75957-003
Proprietary Name:
Boogie Bottoms
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
75957
Start Marketing Date: [9]
06-01-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 75957-003?

The NDC code 75957-003 is assigned by the FDA to the product Boogie Bottoms which is product labeled by Nehemiah Manufacturing Company Llc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 75957-003-01 49 ml in 1 bottle , 75957-003-02 3 bottle in 1 cello pack / 49 ml in 1 bottle (75957-003-01), 75957-003-03 4 bottle in 1 cello pack / 49 ml in 1 bottle (75957-003-01), 75957-003-04 1 bottle in 1 box / 49 ml in 1 bottle (75957-003-01). 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 Boogie Bottoms?

Change wet and soiled diapers promptly.Cleanse diaper area and allow to dry.Shake bottle well before use. Unlock to spray.Re-lock when not in use.Spray 4-6 inches from skin. No rub-in is required.Apply liberally as often as necessary, with each diaper change, especially at bedtime or anytime when exposure to wet diapers may be prolonged.

Which are Boogie Bottoms UNII Codes?

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

Which are Boogie Bottoms 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:

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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".