NDC 54157-102 Megafresh

NDC Product Code 54157-102

NDC 54157-102-01

Package Description: 17 g in 1 TUBE

NDC 54157-102-02

Package Description: 24 g in 1 TUBE

NDC 54157-102-03

Package Description: 35 g in 1 TUBE

NDC 54157-102-04

Package Description: 43 g in 1 TUBE

NDC 54157-102-05

Package Description: 50 g in 1 TUBE

NDC 54157-102-06

Package Description: 70 g in 1 TUBE

NDC 54157-102-07

Package Description: 78 g in 1 TUBE

NDC 54157-102-08

Package Description: 90 g in 1 TUBE

NDC 54157-102-09

Package Description: 100 g in 1 TUBE

NDC 54157-102-10

Package Description: 120 g in 1 TUBE

NDC 54157-102-11

Package Description: 130 g in 1 TUBE

NDC 54157-102-12

Package Description: 150 g in 1 TUBE

NDC 54157-102-13

Package Description: 181 g in 1 TUBE

NDC 54157-102-14

Package Description: 200 g in 1 TUBE

NDC 54157-102-15

Package Description: 4.25 g in 1 POUCH

NDC 54157-102-16

Package Description: 3 g in 1 POUCH

NDC 54157-102-17

Package Description: 5 g in 1 POUCH

NDC 54157-102-18

Package Description: 10 g in 1 POUCH

NDC 54157-102-19

Package Description: 71 g in 1 TUBE

NDC 54157-102-20

Package Description: 85 g in 1 TUBE

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

NDC Product Information

Megafresh with NDC 54157-102 is a product labeled by American Amenities, Inc.. 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: 245598.

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)
  • SORBITOL (UNII: 506T60A25R)
  • POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
  • CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
  • SODIUM LAURYL SULFATE (UNII: 368GB5141J)
  • CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
  • HYDRATED SILICA (UNII: Y6O7T4G8P9)
  • SACCHARIN SODIUM (UNII: SB8ZUX40TY)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)

Product Labeler Information

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

Labeler Name: American Amenities, Inc.
Labeler Code: 54157
Start Marketing Date: 11-04-2013 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 - 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".

* Please review the disclaimer below.

Information for Patients

Fluoride

Fluoride is pronounced as (floor' ide)

Why is fluoride medication prescribed?
Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usu...
[Read More]

* Please review the disclaimer below.

Megafresh Product Label Images

Megafresh Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Active Ingredient

Active Ingredient: Sodium Fluoride (0.22%)

Otc - Purpose

Purpose: Anticavity

Indications & Usage

Uses: Aids in the prevention of dental cavities

Warnings

For external use only. Keep out of reach of children

Otc - Keep Out Of Reach Of Children

Keep out of reach of children under six years of age

Otc - Ask Doctor

If more than used for brushing is accidentally swallowed, get medical help or contact a poison control center immediately.

Dosage & Administration

Adults and children of two years of age and older: Brush teeth thoroughly, perferrably after each meal or at least twice a day, or as directed by a dentist or a doctor. Instruct children under six years of age in good brushing and rinsing habit (to minimize swollowing). Supervise children as necessary until capable of using without supervision. Children under 2 years of age: consult a dentist or doctor.

Inactive Ingredient

Purified Water,Sorbitol, Polyethylene Glycol 1500, Carboxymethylcellulose Sodium, Sodium Lauryl Sulfate, Flavour, Carbomer Homopolymer Type C, Hydrated Silica, Saccharin Sodium,Methylparaben, Propylparaben

* Please review the disclaimer below.