Label: ALBA NATURAL ACNEDOTE ASTRINGENT- salicylic acid lotion
- NDC Code(s): 61995-2753-6
- Packager: The Hain Celestial Group, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 31, 2024
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WARNINGS
For external use only. 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 thoroughly with water.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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INGREDIENTS AND APPEARANCE
ALBA NATURAL ACNEDOTE ASTRINGENT
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61995-2753 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 g Inactive Ingredients Ingredient Name Strength ARNICA MONTANA FLOWER WATER (UNII: U7L2JP51PR) WATER (UNII: 059QF0KO0R) MYRICA ESCULENTA FRUIT (UNII: JKM8M5F55D) LINALOOL, (+)- (UNII: F4VNO44C09) ALOE VERA LEAF (UNII: ZY81Z83H0X) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ) SORBITOL (UNII: 506T60A25R) SODIUM BENZOATE (UNII: OJ245FE5EU) LIMONENE, (+)- (UNII: GFD7C86Q1W) ALCOHOL 95% (UNII: 7528N5H79B) ORANGE PEEL (UNII: TI9T76XD44) PEPPERMINT OIL (UNII: AV092KU4JH) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) TERT-BUTYL ALCOHOL (UNII: MD83SFE959) GLYCERIN (UNII: PDC6A3C0OX) FILIPENDULA ULMARIA WHOLE (UNII: 3LH0M209LN) MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) LAVENDER OIL (UNII: ZBP1YXW0H8) WILLOW BARK (UNII: S883J9JDYX) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) DENATONIUM BENZOATE (UNII: 4YK5Z54AT2) CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61995-2753-6 177 g in 1 BOTTLE; Type 0: Not a Combination Product 07/20/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 01/21/2010 Labeler - The Hain Celestial Group, Inc. (117115556) Registrant - The Hain Celestial Group, Inc. (014334364)