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Boudreauxs - Medication Information

Product NDC Code 0132-0323
Drug Name

Boudreauxs

Type Brand
Active Ingredients
Zinc oxide 40 g/113g
Route TOPICAL
Dosage Form CREAM
Application Number M016
Labeler Name C.B. Fleet Company, Inc.
Packages
Package NDC Code Description
0132-0323-14 397 g in 1 jar (0132-0323-14)
0132-0323-22 57 g in 1 tube (0132-0323-22)
0132-0323-44 113 g in 1 tube (0132-0323-44)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Zinc Oxide, 40%

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 for Use Change wet and soiled diaper immediately Cleanse the diaper area and allow to dry Apply ointment liberally and as often as necessary with each diaper change and especially when exposed to wet diapers for a prolonged period of time, such as bedtime

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Castor Oil, Mineral Oil, Paraffin, Peruvian Balsam, Petrolatum

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.
Uses Helps treat and prevent diaper rash Protects chafed skin due to diaper rash and helps seal out wetness

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Boudreauxs Zinc Oxide ZINC OXIDE ZINC OXIDE CASTOR OIL MINERAL OIL PARAFFIN BALSAM PERU PETROLATUM

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.
PRINCIPAL DISPLAY PANEL TREATS & PROTECTS BOUDREAUX’S BUTT PASTE MAX STRENGTH NET WT. 2 OZ (57 g) TREATS & PROTECTS BOUDREAUX’S BUTT PASTE MAX STRENGTH NET WT. 2 OZ (57 g) PRINCIPAL DISPLAY PANEL BOUDREAUX’S BUTT PASTE Zinc oxide 40% MAX STRENGTH NET WT. 14 OZ (396 g) BOUDREAUX’S BUTT PASTE Zinc oxide 40% MAX STRENGTH NET WT. 14 OZ (396 g)

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.
BOUDREAUXS- zinc oxide cream C.B. Fleet Company, Inc. Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies. ---------- Drug Facts

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 Keep out of reach of children to prevent accidental ingestion If swallowed, seek medical help or call Poison Control Center immediately

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other Information Store at room temperature, 20C to 27C (68F to 80F) Remove foil seal from the tube's tip Use with infants, children and adults Will stain clothing and fabric

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or Comments Call toll free 1-855-785-2888 website www.buttpaste.com

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor Stop use and ask a doctor if condition worsens or does not improve after 7 days

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 For external use only When using this product avoid contact with the eyes

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