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Product NDC Code | 70764-105 | ||||
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Drug Name | Acne spot treatment |
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Type | Brand | ||||
Active Ingredients |
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Route | TOPICAL | ||||
Dosage Form | GEL | ||||
RxCUI drug identifier | 346298 | ||||
Application Number | part333D | ||||
Labeler Name | CONTROL CORRECTIVE SKINCARE INC | ||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.ACTIVE INGREDIENTS 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 APPLY A SMALL AMOUNT WITH FINGERS TO CLEAN, DRY SKIN. MAY BE USED ALL OVER THE AFFECTED AREA OR USED TO SPOT TREAT BLEMISHES. IF ANY DISCOMFORT OCCURS, REDUCE FREQUENCY OR DISCONTINUE USE.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.INACTIVE INGREDIENTS WATER, GLYCOLIC ACID (3%), SD ALCOHOL 40-A, ALOE BARBADENSIS LEAF JUICE, WITCH HAZEL, GLYCERIN, TRIETHANOLAMINE, METHYL GLUCETH-20, SODIUM LACTATE, FRUCTOSE, UREA, NIACINAMIDE, INOSITOL, SODIUM BENZOATE, LACTIC ACID, HYDROXYETHYLCELLULOSE, PHENOXYETHANOL, PANTHENOL, ALLANTOIN, GLUCOSAMINE SULFATE, METHYLISOTHIAZOLINONE.
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 AN EXFOLIATING GEL THAT AIDS IN REDUCING ACNE BREAKOUTS.
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.ACNE SPOT TREATMENT SALICYLIC ACID WATER GLYCOLIC ACID ALCOHOL ALOE VERA LEAF WITCH HAZEL GLYCERIN TROLAMINE METHYL GLUCETH-20 SODIUM LACTATE SODIUM PYRROLIDONE CARBOXYLATE FRUCTOSE UREA NIACINAMIDE INOSITOL SODIUM BENZOATE LACTIC ACID HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) PHENOXYETHANOL PANTHENOL ALLANTOIN GLUCOSAMINE SULFATE METHYLISOTHIAZOLINONE SALICYLIC ACID SALICYLIC ACID
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.01b UC_Acne Spot Treatment
Do not use
Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.DO NOT USE IF ALLERGIC TO ASPERIN.
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.
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: WWW.CONTROLCORRECTIVE.COM TOLL FREE 1-866-290-4290 MADE IN USA
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. DO NOT USE ON BROKEN SKIN. AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER.
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