NDC 69804-018 Extra Strength Pretat

NDC Product Code 69804-018

NDC CODE: 69804-018

Proprietary Name: Extra Strength Pretat What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

NDC Code Structure

NDC 69804-018-10

Package Description: 28350 mg in 1 JAR

NDC 69804-018-11

Package Description: 56699 mg in 1 JAR

NDC 69804-018-12

Package Description: 113398 mg in 1 JAR

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Extra Strength Pretat with NDC 69804-018 is a product labeled by Ridge Properties. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1010077.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • COPAIBA OIL (UNII: 64VX45Y68N)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • PIPER METHYSTICUM ROOT (UNII: BOW48C81XP)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Ridge Properties
Labeler Code: 69804
Start Marketing Date: 08-17-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 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.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. 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".

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