Label: BACK-UP PLAN ACNE-CONTROL BODY MIST- salicylic acid spray
- NDC Code(s): 73690-023-01
- Packager: Offspring Beauty Co.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 4, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only.
When using this product
- skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
- avoid spraying into eyes. contents under pressure. do not puncture or incinerate. do not store at temperature above 120°F/50°C.
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Directions
- clean skin thoroughly before applying this product
- spray to cover the entire affected area of the back 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
- sensitivity test for a new user: apply product sparingly to one or two small affected areas during first 3 days. if no discomfort occurs, follow directions above.
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Inactive ingredients
Water/Aqua/Eau, Dipropylene Glycol, Polysorbate 20, Hamamelis Virginiana (Witch Hazel) Water, Glycereth-7 Trimethyl Ether, Glycereth-26, Methyl Gluceth-20, Sodium Hydroxide, Glycerin, Phenoxyethanol, Panthenol, Sodium Benzoate, Allantoin, Butylene Glycol, Disodium EDTA, Ethylhexylglycerin, Dipotassium Glycyrrhizate, Benzoic Acid, Sodium Hyaluronate, Citric Acid, Melaleuca Alternifolia (Tea Tree) Leaf Extract, Oenothera Biennis (Evening Primrose) Oil, Glycyrrhiza Glabra (Licorice) Root Extract.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 100 ml Bottle Label
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INGREDIENTS AND APPEARANCE
BACK-UP PLAN ACNE-CONTROL BODY MIST
salicylic acid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73690-023 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIPROPYLENE GLYCOL (UNII: E107L85C40) POLYSORBATE 20 (UNII: 7T1F30V5YH) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) GLYCERETH-7 TRIMETHYL ETHER (UNII: XMC7402M60) GLYCERETH-26 (UNII: NNE56F2N14) METHYL GLUCETH-20 (UNII: J3QD0LD11P) SODIUM HYDROXIDE (UNII: 55X04QC32I) GLYCERIN (UNII: PDC6A3C0OX) PHENOXYETHANOL (UNII: HIE492ZZ3T) PANTHENOL (UNII: WV9CM0O67Z) SODIUM BENZOATE (UNII: OJ245FE5EU) ALLANTOIN (UNII: 344S277G0Z) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) HYALURONATE SODIUM (UNII: YSE9PPT4TH) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) EVENING PRIMROSE OIL (UNII: 3Q9L08K71N) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) BENZOIC ACID (UNII: 8SKN0B0MIM) Product Characteristics Color WHITE (Clear/Translucent) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73690-023-01 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 07/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 07/01/2020 Labeler - Offspring Beauty Co. (081516405) Establishment Name Address ID/FEI Business Operations KDC/One Chatsworth, Inc. 118542196 MANUFACTURE(73690-023)