NDC 69804-020 Extra Strength Aftertat Slime

NDC Product Code 69804-020

NDC 69804-020-14

Package Description: 28500 mg in 1 JAR

NDC 69804-020-15

Package Description: 56700 mg in 1 JAR

NDC 69804-020-16

Package Description: 113400 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 Aftertat Slime with NDC 69804-020 is a product labeled by Ridge Properties. The generic name of Extra Strength Aftertat Slime is . The product's dosage form is and is administered via form.

Labeler Name: Ridge Properties

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

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.

  • FLAX SEED (UNII: 4110YT348C)
  • WITCH HAZEL (UNII: 101I4J0U34)
  • WALNUT OIL (UNII: Y0P3555R51)
  • ALMOND OIL (UNII: 66YXD4DKO9)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)
  • COCONUT OIL (UNII: Q9L0O73W7L)
  • ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
  • COPAIBA OIL (UNII: 64VX45Y68N)
  • NUTMEG OIL (UNII: Z1CLM48948)
  • MORINGA OLEIFERA LEAF OIL (UNII: 89D604766N)
  • ROSA CANINA FLOWER OIL (UNII: DUY7M48I1T)

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: 01-13-2017 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: 12-31-2018 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 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. Values = ‘Y’ or ‘N’.

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