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Nas max strength spot treatment - Medication Information

Product NDC Code 26052-022
Drug Name

Nas max strength spot treatment

Type Brand
Active Ingredients
Salicylic acid 2 g/100g
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 317152
Application Number part333D
Labeler Name BURT'S BEES, INC.
Packages
Package NDC Code Description
26052-022-01 1 tube in 1 carton (26052-022-01) / 10 g in 1 tube
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENT SALICYLIC ACID 2.0%

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 CLEANSE THE SKIN THOROUGHLY BEFORE APPLYING MEDICATION. ON ANY AND ALL ACTIVE BLEMISHES, START WITH ONE APPLICATION DAILY THEN GRADUALLY INCREASE TO 2 OR 3 APPLICATIONS DAILY IF NEEDED. IF BOTHERSOME DRYNESS OR PEELING OCCURS, REDUCE APPLICATION TO ONCE A DAY OR EVERY OTHER DAY.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
INACTIVE INGREDIENTS WATER, CAPRYLIC/CAPRIC TRIGLYCERIDE, GLYCERIN, SALIX NIGRA (WILLOW) BARK EXTRACT, STEARYL ALCOHOL, CETYL ALCOHOL, GLYCERYL STEARATE, BEESWAX, CALOPHYLLUM INOPHYLLUM SEED OIL, CYMBOPOGON SCHOENANTHUS EXTRACT, DIPOTASSIUM GLYCYRRHIZATE, EQUSETUM HIEMALE EXTRACT, HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF EXTRACT, HUMULUS LUPULUS (HOPS) EXTRACT, HYDRASTIS CANADENSIS (GOLDENSEAL) EXTRACT, LONICERA CAPRIFULIUM EXTRACT, LONICERA JAPONICA EXTRACT, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, STEARIC ACID, SORBIC ACID, TOCOPHEROL, XANTHAN GUM, LECITHIN, GLUCOSE, GLYCINE SOJA (SOYBEAN) OIL, FRAGRANCE, SODIUM CHLORIDE, GLUCOSE OXIDASE, LACTOPEROXIDASE, PHENOXYETHANOL.

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 PENETRATES PORES TO CONTROL ACNE.

Purpose

Information about the drug product’s indications for use.
PURPOSE ACNE TREATMENT

Spl product data elements

Usually a list of ingredients in a drug product.
NAS MAX STRENGTH SPOT TREATMENT SALICYLIC ACID CYMBOPOGON SCHOENANTHUS TOP SIMMONDSIA CHINENSIS SEED SALICYLIC ACID SALICYLIC ACID GLYCERYL STEARATE SE PHENOXYETHANOL TOCOPHEROL SOYBEAN OIL STEARYL ALCOHOL SALIX NIGRA BARK WATER GLYCERIN CETYL ALCOHOL WHITE WAX TAMANU OIL GLYCYRRHIZINATE DIPOTASSIUM HAMAMELIS VIRGINIANA LEAF STEARIC ACID HUMULUS LUPULUS WHOLE HYDRASTIS CANADENSIS WHOLE LONICERA CAPRIFOLIUM FLOWER LECITHIN, SOYBEAN GLUCOSE OXIDASE LACTOPEROXIDASE BOVINE XANTHAN GUM MEDIUM-CHAIN TRIGLYCERIDES LONICERA JAPONICA FLOWER POTASSIUM STEARATE

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.
PDP BURT'S BEES NATURAL ACNE SOLUTIONS MAXIMUM STRENGTH SPOT TREATMENT CREAM NET WT. 0.5 OZ. 10 G ACNE MAX SPOT

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 CALL 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? 800-849-7112 OR WWW.BURTSBEES.COM

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. USING OTHER TOPICAL ACNE MEDICATION AT THE SAME TIME OR IMMEDIATELY FOLLOWING USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS DIRECTED BY A DOCTOR. KEEP OUT OF REACH OF CHILDREN IF SWALLOWED, GET MEDICAL HELP OR CALL 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