Label: ST. IVES BLEMISH AND BLACKHEAD CONTROL APRICOT SCRUB- solutions acne control spot treatment lotion
- NDC Code(s): 64942-1861-1
- Packager: CONOPCO Inc. d/b/a Unilever
- 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 7, 2022
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- Official Label (Printer Friendly)
- ST. IVES SOLUTIONS ACNE CONTROL SPOT TREATMENT - (Salicylic Acid) lotion
- Active ingredient
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
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Directions
Cleanse skin thoroughly before applying product
Cover the entire affected area with a thin layer one to three times daily
Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily, if needed or as directed by a doctor.
If bothersome dryness or peeling occurs, reduce application to once a day or every other day. - Other information
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Inactive ingredients
Water (Aqua), Cellulose, Caprylic/Capric Triglyceride, Steareth-2, Glycerin, Magnesium Aluminum Silicate, Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, Steareth-21, Phenoxyethanol, Jojoba Esters, Menthol, Xanthan Gum, Helianthus Annuus (Sunflower) Seed Wax, Sodium Phytate, Niacinamide, Polyglycerin-3, Acacia Decurrens Flower Wax, Tasmannia Lanceolata Fruit/Leaf Extract, Butylene Glycol, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Melaleuca Alternifolia (Tea Tree) Flower/Leaf/Stem Extract.
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- Packaging
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INGREDIENTS AND APPEARANCE
ST. IVES BLEMISH AND BLACKHEAD CONTROL APRICOT SCRUB
solutions acne control spot treatment lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1861 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.02 g in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) STEARETH-2 (UNII: V56DFE46J5) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) SHEA BUTTER (UNII: K49155WL9Y) STEARETH-21 (UNII: 53J3F32P58) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) PHENOXYETHANOL (UNII: HIE492ZZ3T) HYDROGENATED JOJOBA OIL, RANDOMIZED (UNII: Q47ST02F58) MENTHOL (UNII: L7T10EIP3A) XANTHAN GUM (UNII: TTV12P4NEE) HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV) PHYTATE SODIUM (UNII: 88496G1ERL) NIACINAMIDE (UNII: 25X51I8RD4) POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6) ACACIA DECURRENS FLOWER WAX (UNII: AU6XZE9IY9) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MELALEUCA ALTERNIFOLIA FLOWERING TOP (UNII: 5AZ4S6N66F) HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV) POWDERED CELLULOSE (UNII: SMD1X3XO9M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1861-1 22 g in 1 TUBE; Type 0: Not a Combination Product 07/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 07/01/2021 Labeler - CONOPCO Inc. d/b/a Unilever (001375088)
