Label: ANTI-AGING BLEMISH CONTROL CLEANSER- salicylic acid liquid
- NDC Code(s): 65278-106-02, 65278-106-05
- Packager: June Jacobs Labs, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated May 14, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
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 irrtitation of the skin. If this occurs, only one medication should be used unless directed by a doctor.
- Avoid contact with eyes. If excessive skin irritation develops or increases, discontinue use and consult a doctor.
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive Ingredients
Water/ Aqua, Glycerin, Propanediol, Decyl Glucoside, Fragrance/Parfum, Sodium Levulinate, Salix Nigra (Willow) Bark Extract, Lactic Acid, Sodium Anisate, Allantoin, Panthenol, Sodium Phytate, Ascophyllum Nodosum Extract, Curcuma Longa (Turmeric) Root Extract, Sodium Hydroxide, Chlorella Vulgaris Extract, Globularia Alypum Leaf Extract, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Lycium Barbarum Fruit Extract, Punica Granatum Extract, Vitis Vinifera (Grape) Seed Extract, Aspalathus Linearis Leaf Extract, Menthol, Camphor, Malic Acid, Alginic Acid,Arnica Montana Flower Extract, Leuconostoc/Radish Root Ferment Filtrate, Helianthus Annuus (Sunflower) Seed Oil, Hyaluronic Acid, Phenoxyethanol, Alcohol, Brassica Oleracea Italica (Broccoli) Extract, Chamomilla Recutita (Matricaria) Flower Extract, Camellia Sinensis Leaf Extract, Potassium Sorbate, Sodium Benzoate, Tocopherol, Limonene, Linalool, Benzyl Benzoate, Eugenol, Citral, Geraniol
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ANTI-AGING BLEMISH CONTROL CLEANSER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65278-106 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1.4787 g in 147.87 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CARYOPHYLLENE (UNII: BHW853AU9H) GLYCERIN (UNII: PDC6A3C0OX) CLOVE LEAF OIL (UNII: VCA5491KVF) CHLORELLA VULGARIS (UNII: RYQ4R60M02) MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G) PUNICA GRANATUM ROOT BARK (UNII: CLV24I3T1D) SODIUM BENZOATE (UNII: OJ245FE5EU) LEMON OIL (UNII: I9GRO824LL) SODIUM LEVULINATE (UNII: VK44E1MQU8) 3-HEXEN-1-OL, (3Z)- (UNII: V14F8G75P4) GERANIOL (UNII: L837108USY) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) BROCCOLI SPROUT (UNII: 128UH9LOAE) ALCOHOL (UNII: 3K9958V90M) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) TOCOPHEROL (UNII: R0ZB2556P8) MALIC ACID (UNII: 817L1N4CKP) ALGINIC ACID (UNII: 8C3Z4148WZ) HYALURONIC ACID (UNII: S270N0TRQY) CHAMOMILE (UNII: FGL3685T2X) PHYTATE SODIUM (UNII: 88496G1ERL) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) ALLANTOIN (UNII: 344S277G0Z) TURMERIC (UNII: 856YO1Z64F) SODIUM HYDROXIDE (UNII: 55X04QC32I) VITIS VINIFERA SEED (UNII: C34U15ICXA) LINALYL ACETATE (UNII: 5K47SSQ51G) LINALOOL, (+/-)- (UNII: D81QY6I88E) SALIX NIGRA BARK (UNII: QU52J3A5B3) GREEN TEA LEAF (UNII: W2ZU1RY8B0) EUGENOL (UNII: 3T8H1794QW) BENZYL BENZOATE (UNII: N863NB338G) SODIUM ANISATE (UNII: F9WFJ28MV9) ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ) LYCIUM BARBARUM FRUIT (UNII: 930626MWDL) CAMPHOR (NATURAL) (UNII: N20HL7Q941) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPANEDIOL (UNII: 5965N8W85T) ORANGE OIL (UNII: AKN3KSD11B) MANDARIN OIL (UNII: NJO720F72R) GINGER OIL (UNII: SAS9Z1SVUK) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) CITRAL (UNII: T7EU0O9VPP) CITRONELLA OIL (UNII: QYO8Q067D0) PANTHENOL (UNII: WV9CM0O67Z) GLOBULARIA CORDIFOLIA WHOLE (UNII: SD327VQ78H) ASPALATHUS LINEARIS LEAF (UNII: H7UGK1GJCU) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) SUNFLOWER OIL (UNII: 3W1JG795YI) LIMONENE, (+)- (UNII: GFD7C86Q1W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65278-106-05 147.87 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 04/08/2010 2 NDC:65278-106-02 147.87 g in 1 CARTON; Type 0: Not a Combination Product 04/08/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 04/08/2010 Labeler - June Jacobs Labs, LLC (082439410) Establishment Name Address ID/FEI Business Operations June Jacobs Labs, LLC 122610681 manufacture(65278-106)