Label: ANTI-AGING BLEMISH CONTROL PEEL PADS- salicylic acid swab
- NDC Code(s): 65278-318-01, 65278-318-02
- Packager: June Jacobs Labs, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 21, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions
■ On clean, dry skin, smooth applicator over affected area, avoiding contact with eyes
■ Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two 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.
■ Follow with moisturizer and sunscreen during the day.
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INACTIVE INGREDIENT
Inactive ingredients
Water/Aqua/Eau, Alcohol Denat., Butylene Glycol, Glycolic Acid, Glycerin, Sodium Hydroxide, Salix Nigra (Willow) Bark Extract, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Fragrance/ Parfum, Pentylene Glycol, Lecithin, Lycium Barbarum Fruit Extract, Punica Granatum Extract, Vitis Vinifera (Grape) Seed Extract, Aspalathus Linearis Leaf Extract, Camphor, Menthol, Globularia Alypum Leaf Extract, Retinol, Polysorbate 20, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Aloe Barbadensis Leaf Juice, Leuconostoc/Radish Root Ferment Filtrate, Lactic Acid, Ascophyllum Nodosum Extract, Potassium Phosphate, Helianthus Annuus (Sunflower) Seed Oil, Malto dextrin, Camellia Sinensis Leaf Extract, Brassica Oleracea Italica (Broccoli) Extract, Malic Acid, Alginic Acid, BHT, BHA, Tocopherol , Ascorbyl Palmitate, Limonene, Linalool, Benzyl Benzoate, Eugenol, Citral, Geraniol
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTI-AGING BLEMISH CONTROL PEEL PADS
salicylic acid swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65278-318 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2.366 g in 118.29 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) CARYOPHYLLENE (UNII: BHW853AU9H) GLYCOLIC ACID (UNII: 0WT12SX38S) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) GLOBULARIA CORDIFOLIA WHOLE (UNII: SD327VQ78H) PENTYLENE GLYCOL (UNII: 50C1307PZG) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) MALTODEXTRIN (UNII: 7CVR7L4A2D) MALIC ACID (UNII: 817L1N4CKP) ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ) SUNFLOWER OIL (UNII: 3W1JG795YI) TOCOPHEROL (UNII: R0ZB2556P8) BENZYL BENZOATE (UNII: N863NB338G) LEMON OIL (UNII: I9GRO824LL) ORANGE OIL (UNII: AKN3KSD11B) CITRAL (UNII: T7EU0O9VPP) GERANIOL (UNII: L837108USY) ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU) 3-HEXEN-1-OL, (3Z)- (UNII: V14F8G75P4) SODIUM HYDROXIDE (UNII: 55X04QC32I) SALIX NIGRA BARK (UNII: QU52J3A5B3) CLOVE LEAF OIL (UNII: VCA5491KVF) VITIS VINIFERA SEED (UNII: C34U15ICXA) ASCORBYL PALMITATE (UNII: QN83US2B0N) MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G) ALGINIC ACID (UNII: 8C3Z4148WZ) LIMONENE, (+)- (UNII: GFD7C86Q1W) ALCOHOL (UNII: 3K9958V90M) MANDARIN OIL (UNII: NJO720F72R) LINALYL ACETATE (UNII: 5K47SSQ51G) POLYSORBATE 20 (UNII: 7T1F30V5YH) POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632) BROCCOLI SPROUT (UNII: 128UH9LOAE) LYCIUM BARBARUM FRUIT (UNII: 930626MWDL) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CITRONELLA OIL (UNII: QYO8Q067D0) RETINOL (UNII: G2SH0XKK91) GREEN TEA LEAF (UNII: W2ZU1RY8B0) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) WATER (UNII: 059QF0KO0R) PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P) GINGER OIL (UNII: SAS9Z1SVUK) LINALOOL, (+/-)- (UNII: D81QY6I88E) MENTHOL (UNII: L7T10EIP3A) ALOE VERA LEAF (UNII: ZY81Z83H0X) LACTIC ACID (UNII: 33X04XA5AT) PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65278-318-01 118.29 g in 1 JAR; Type 0: Not a Combination Product 06/20/2012 2 NDC:65278-318-02 118.29 g in 1 CARTON; Type 0: Not a Combination Product 06/20/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 06/20/2012 Labeler - June Jacobs Labs, LLC (082439410) Establishment Name Address ID/FEI Business Operations June Jacobs Labs, LLC 122610681 manufacture(65278-318)