Label: NATURES CURE BODY ACNE TREATMENT- salicylic acid spray
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Contains inactivated NDC Code(s)
NDC Code(s): 21839-680-01 - Packager: Gordon Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 Label Information
Updated December 30, 2019
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- Official Label (Printer Friendly)
- Drug Facts
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS AND PRECAUTIONS
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WHEN USING
When using this product
* Using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin. If this occurs, only one drug should be used unless directed by a doctor.
* Do not spray directly on or near face.
* Avoid contact with eyes, lips and mouth.
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions * Cleanse skin thoroughly.
*Spray the entire affected area with a thin layer 1 to 3 times daily.
*Because excessive drying of the skin may occur, gradually increase to 2 or 3 times daily if needed or as directed by a doctor.
* Leave on all day or night.
* If bothersome dryness or peeling occurs, reduce usage to once a day or every other day.
* To use on face, spray onto cotton ball and brush onto skin.
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DESCRIPTION
Nature's Cure clears and prevents acne on your back, chest, neck and arms. The maximum strength formula sprays from any angle, even upside down, to treat hard-to-reach places. It fights acne caused by sweating and friction from athletic gear and clothing. The non-staining spray contains moisturizing botanicals that help soothe skin.
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INACTIVE INGREDIENT
Allantoin, Aloe Barbadensis Leaf Juice, Arctium Majus Root Extract (Burdock), Calendula Officinalis Flower Extract, Capryloyl Glycine, Chamomilla Recutita (Matricaria) Flower Extract, Cinnamomum Zeylanicum Bark Water Extract, Fragrance, Hamamelis Virginiana (Witch Hazel) Extract, Methylparaben, Phospholipids, Propylene Glycol, Propylparaben, Salix Nigra (Willow) Bark Extract, Sarcosine, SD Alcohol 40, Sodium Citrate, Tocopheryl Acetate (Vitamin E), Triethanolamine, Water (Aqua).
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INGREDIENTS AND APPEARANCE
NATURES CURE BODY ACNE TREATMENT
salicylic acid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21839-680 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) METHYLPARABEN (UNII: A2I8C7HI9T) HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY) CINNAMON BARK OIL (UNII: XE54U569EC) CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) WATER (UNII: 059QF0KO0R) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) SALIX NIGRA BARK (UNII: QU52J3A5B3) PROPYLPARABEN (UNII: Z8IX2SC1OH) SODIUM CITRATE (UNII: 1Q73Q2JULR) TROLAMINE (UNII: 9O3K93S3TK) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ALCOHOL (UNII: 3K9958V90M) SARCOSINE (UNII: Z711V88R5F) CHAMOMILE (UNII: FGL3685T2X) ALOE VERA LEAF (UNII: ZY81Z83H0X) ALLANTOIN (UNII: 344S277G0Z) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21839-680-01 103 mL in 1 BOTTLE; Type 0: Not a Combination Product 06/20/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/20/2016 Labeler - Gordon Laboratories, Inc. (008328619) Registrant - Gordon Laboratories, Inc. (008328619) Establishment Name Address ID/FEI Business Operations GORDON LABORATORIES, INC 008328619 manufacture(21839-680)