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Antiperspirant wipe for women - Medication Information

Product NDC Code 71592-001
Drug Name

Antiperspirant wipe for women

Type Brand
Active Ingredients
Aluminum chlorohydrate 15 g/100g
Route TOPICAL
Dosage Form SWAB
Application Number part350
Labeler Name FlawlessWipes, LLC
Packages
Package NDC Code Description
71592-001-86 6 packet in 1 package (71592-001-86) / 3 g in 1 packet (71592-001-85)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENT Aluminum Chlorohydrate 15%

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 Open packet, remove and unfold wipe, apply to underarm only, dispose of used wipe in the trash, do not flush.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water, polysorbate 20, Salvia Officinalis (Sage) Leaf Extract, Usnea Barbata (Lichen) extract, Tocopherol, Tocopheryl Acetate, PEG-180, Phenoxyethanol, Benzyl Alcohol, Potassium Sorbate, Fragrance

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 Underarm antiperspirant to reduce perspiration and odor

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Antiperspirant Wipe for Women Aluminum Chlorohydrate ALUMINUM CHLOROHYDRATE ALUMINUM CHLOROHYDRATE Water USNEA BARBATA TOCOPHEROL .ALPHA.-TOCOPHEROL ACETATE, DL- SAGE POTASSIUM SORBATE POLYSORBATE 20 PHENOXYETHANOL BENZYL ALCOHOL POLYETHYLENE GLYCOL 8000

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.
Pakaging Label

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 If swallowed, get medical help or contact a poison control center right away

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 eyes. in case of eye contact, flush thoroughly with water. Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours

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