NDC 18027-033 Pharmacys Prescription

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:
18027-033
Proprietary Name:
Pharmacys Prescription
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
18027
Start Marketing Date: [9]
10-01-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 18027-033?

The NDC code 18027-033 is assigned by the FDA to the product Pharmacys Prescription which is product labeled by American Consumer Products Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 18027-033-10 296 g in 1 bottle, spray , 18027-033-12 3785 g in 1 bottle, plastic , 18027-033-16 473 g in 1 bottle, plastic . 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 Pharmacys Prescription?

First aid antiseptic:clean affected areaapply small amount of product on affected area 1-3 times a daymay be covered with a sterile bandageif bandage, let dry firstoral debriding agent (oral rinse):adults and children 2 years of age or over:mix with an equal amount of waterswish around in the mouth over affected area for atleast 1 minute then spit outuse up to 4x daily after meals and at bedtime or as directed by a dentist or doctorchildren under 12 years should be supervised in the use of this productchildren under 2 years of age; consult a dentist or doctor

Which are Pharmacys Prescription UNII Codes?

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

Which are Pharmacys Prescription 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:

What is the NDC to RxNorm Crosswalk for Pharmacys Prescription?

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".