Label: AL0076900 ALBA BOTANICA ACNEDOTECLEARING PEEL- salicylic acid gel
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Contains inactivated NDC Code(s)
NDC Code(s): 61995-2769-4 - Packager: The Hain Celestial Group, 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 April 12, 2021
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- ACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- PURPOSE
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WARNINGS
Using other topical acne medications at the same time or immediately following the 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. Avoid direct contact with eyes. If contact occurs, flush throughly with water.
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
Aloe Barbadensis Leaf Juice(1), Water,Glycerin, Alcohol (1), Vaccinium Myrtillus Fruit Extract, Xanthan Gum, Saccharum Officinarum (Sugar Cane) Extract ,Citrus Aurantium Bergamia (Bergamot) Fruit Oil (1), Acer Saccharum (Sugar Maple) Extract, Algae Extract, Citrus Aurantium Dulcis (Orange) Fruit Extract, Citrus Limon (Lemon) Fruit Extract, Fragaria Vesca (Strawberry) Fruit Extract (1), Lactobacillus/Arundinaria Ferment Filtrate, Leuconostoc/Radish Root Ferment Filtrate, Olea Europaea (Olive) Leaf Extract, Panax Ginseng Root Extract, Purys Malus (Apple) Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Salix Alba (Willow) Bark Extract (1), Vitis Vinifera(Grape) Fruit Extract, Citric Acid, Tocopheryl Acetate, Bentonite, Lactic Acid, Potassium Hydroxide, Quartz, Sea Salt, Sodium Phytate,Alcohol, Ethylhexylglycerine, Phenoxyethanol, Sodium Benzoate, Potassium Sorbate, BenzylAlcohol
(1) Certified Organicf Ingredient;
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AL0076900 ALBA BOTANICA ACNEDOTECLEARING PEEL
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61995-2769 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1 g in 100 g Inactive Ingredients Ingredient Name Strength ALPINE STRAWBERRY (UNII: CG6IX3GCMU) ASIAN GINSENG (UNII: CUQ3A77YXI) APPLE (UNII: B423VGH5S9) SALIX ALBA BARK (UNII: 205MXS71H7) WINE GRAPE (UNII: 3GOV20705G) LEMON (UNII: 24RS0A988O) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ACER SACCHARUM BARK/SAP (UNII: Z120VL0KAC) ALOE VERA LEAF (UNII: ZY81Z83H0X) ORANGE (UNII: 5EVU04N5QU) BLACKBERRY (UNII: 8A6OMU3I8L) SUGARCANE (UNII: 81H2R5AOH3) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) ALCOHOL (UNII: 3K9958V90M) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) PHYTATE SODIUM (UNII: 88496G1ERL) BERGAMOT OIL (UNII: 39W1PKE3JI) LACTIC ACID (UNII: 33X04XA5AT) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) BENTONITE (UNII: A3N5ZCN45C) SEA SALT (UNII: 87GE52P74G) OLEA EUROPAEA LEAF (UNII: MJ95C3OH47) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61995-2769-4 113 g in 1 TUBE; Type 0: Not a Combination Product 06/06/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 06/06/2017 Labeler - The Hain Celestial Group, Inc. (117115556) Registrant - The Hain Celestial Group, Inc. (081512382) Establishment Name Address ID/FEI Business Operations The Hain Celestial Group, Inc. 081512382 manufacture(61995-2769)
