Label: BODEWELL PSORIASIS SOOTHING- salicylic acid spray
- NDC Code(s): 69423-616-11
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Directions
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Warnings
For external use only.
When using this product
- avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop use and ask a doctor if
- condition worsens or does not improve after regular use of this product as directed.
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Inactive ingredients
Water, glycerin, niacinamide, phenoxyethanol, sodium hydroxide, aminomethyl propanol, 1,2-hexanediol, caprylyl glycol, sodium citrate, polysorbate 20, citric acid, alcohol, hamamelis virginiana (witch hazel) bark/leaf extract, avena sativa (oat) seed extract, populus alba bark extract, populus tremuloides bark extract, cochlearia officinalis flower/leaf/stalk extract, phytolacca decandra root extract, lens esculenta (lentil) fruit extract, berberis vulgaris bark extract, scrophularia nodosa extract, veronica officinalis extract, sanguinaria canadensis rhizome/root extract, althaea officinalis root extract, chamomilla recutita (matricaria) flower extract, sambucus nigra extract, achillea millefolium extract, aesculus hippocastanum (horse chestnut) seed extract, malva sylvestris (mallow) leaf extract, nasturtium officinale leaf extract, smilax medica root extract, tussilago farfara (coltsfoot) leaf extract, pimpinella saxifraga extract, vincetoxicum hirundinaria root extract.
- Questions (or comments)?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 118 mL Bottle
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INGREDIENTS AND APPEARANCE
BODEWELL PSORIASIS SOOTHING
salicylic acid sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-616 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1.8 g in 100 mL Inactive Ingredients Ingredient Name Strength 1,2-HEXANEDIOL (UNII: TR046Y3K1G) SODIUM HYDROXIDE (UNII: 55X04QC32I) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER) POLYSORBATE 20 (UNII: 7T1F30V5YH) POPULUS TREMULOIDES BARK (UNII: 5543O0CEID) SODIUM CITRATE (UNII: 1Q73Q2JULR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) COCHLEARIA OFFICINALIS FLOWERING TOP (UNII: M87UN67CKR) SMILAX ARISTOLOCHIIFOLIA ROOT (UNII: NR100Y25G0) SAMBUCUS NIGRA WHOLE (UNII: 4X6JT95SYN) SCROPHULARIA NODOSA (UNII: 7H443NUB2T) POPULUS ALBA BARK (UNII: K12723D3GV) HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY) ACHILLEA MILLEFOLIUM WHOLE (UNII: 2FXJ6SW4PK) HORSE CHESTNUT (UNII: 3C18L6RJAZ) WATER (UNII: 059QF0KO0R) ACHILLEA MILLEFOLIUM SEED (UNII: 8V0N54LMLR) ALCOHOL (UNII: 3K9958V90M) ALTHAEA OFFICINALIS ROOT (UNII: TRW2FUF47H) BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERIN (UNII: PDC6A3C0OX) TUSSILAGO FARFARA LEAF (UNII: G2GH7V846Z) VINCETOXICUM HIRUNDINARIA ROOT (UNII: 9R858U917W) PHENOXYETHANOL (UNII: HIE492ZZ3T) LENS CULINARIS FRUIT (UNII: ZYZ076G9JH) NIACINAMIDE (UNII: 25X51I8RD4) PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) VERONICA OFFICINALIS WHOLE (UNII: 9EHR580PSP) MALVA SYLVESTRIS LEAF (UNII: 17H39B00T5) NASTURTIUM OFFICINALE LEAF (UNII: 362629QKRT) PIMPINELLA SAXIFRAGA WHOLE (UNII: LCL1491142) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-616-11 118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 02/15/2022 04/30/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 02/15/2022 04/30/2024 Labeler - The Procter & Gamble Manufacturing Company (004238200)
