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Heb hebuddy - Medication Information

Product NDC Code 37808-192
Drug Name

Heb hebuddy

Type Brand
Active Ingredients
Sodium fluoride .15 g/100g
Route DENTAL
Dosage Form PASTE, DENTIFRICE
RxCUI drug identifier 891775
Application Number M021
Labeler Name HEB
Packages
Package NDC Code Description
37808-192-02 120 g in 1 tube (37808-192-02)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Sodium Fluoride 0.243%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Adults and children 2 years of age and older: brush teeth thoroughly preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Do not swallow To minimize swallowing use a pea-sized amount in children under 6 Supervise childrens brushing until good habits are established Children under 2 years of age: consult a dentist or doctor.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients sorbitol, water, hydrated silica, glycerin, cellulose gum, PEG-12, flavor, sodium benzoate, sodium saccharin, cocamidopropyl betaine, mica, titanium dioxide, red 40

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Use Helps protect against cavities

Purpose

Information about the drug product’s indications for use.
Purpose Anticavity

Spl product data elements

Usually a list of ingredients in a drug product.
HEB HEBuddy Fluoride MICA GLYCERIN WATER SODIUM BENZOATE SORBITOL TITANIUM DIOXIDE SACCHARIN SODIUM COCAMIDOPROPYL BETAINE HYDRATED SILICA POLYETHYLENE GLYCOL 600 CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM FD&C RED NO. 40 SODIUM FLUORIDE FLUORIDE ION Watermelon mint

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Tube label

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts MADE WITH PRIDE AND CARE FOR H-E-B, SAN ANTONIO, TX 78204 MADE IN USA

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? Call 1-877-777-2743

Storage and handling

Information about safe storage and handling of the drug product.
Other information Store in a cool dry place. Keep tube capped when not in use.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API