Label: ACNE WARRIOR CLEARING ASTRINGENT- salicylic acid liquid
- NDC Code(s): 61197-121-00
- Packager: Pacifica Beauty, LLC
- 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 February 9, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient Purpose
- Use
- Warnings
- INDICATIONS & USAGE
- Keep out of reach of children.
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Directions
Clean the skin thoroughly before applying this 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. Sensitivity test for a new user. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated above.
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Inactive ingredients:
Aqua, Alcohol Denat., Glycerin, Sorbitol, Hamamelis Virginiana (Witch Hazel) Water, Niacinamide, Cucumis Sativus (Cucumber) Fruit Extract*, Aloe Barbadensis Leaf Juice*, Epilobium Angustifolium Flower/Leaf/Stem Extract, Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract*, Chamomilla Recutita (Matricaria) Flower Extract *, Camellia Sinensis (White Tea) Leaf Extract*, Arnica Montana Flower Extract*, Spiraea Ulmaria (Meadowsweet) Extract, Salvia Officinalis (Sage) Oil, Mentha Piperita (Peppermint) Oil, Lens Esculenta (Lentil) Seed Extract, Sodium PCA, Dipotassium Glycyrrhizate, Parfum**. *certified organic **our scent blend with natural and/or essential oils
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- Acne Warrior Clearing Astringent Label
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INGREDIENTS AND APPEARANCE
ACNE WARRIOR CLEARING ASTRINGENT
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61197-121 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 g in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) WATER (UNII: 059QF0KO0R) LAVANDULA ANGUSTIFOLIA WHOLE (UNII: 51217XIL5L) CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9) HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2) EPILOBIUM ANGUSTIFOLIUM WHOLE (UNII: C278QS9YBT) SALVIA OFFICINALIS WHOLE (UNII: M9C36LC10E) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) ALCOHOL (UNII: 3K9958V90M) GLYCERIN (UNII: PDC6A3C0OX) SORBITOL (UNII: 506T60A25R) NIACINAMIDE (UNII: 25X51I8RD4) CUCUMIS SATIVUS WHOLE (UNII: 50560UL2YV) LENTIL (UNII: 6O38V6B52O) CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) MENTHA PIPERITA (UNII: 79M2M2UDA9) GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61197-121-00 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/09/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M006 02/09/2023 Labeler - Pacifica Beauty, LLC (868275517) Establishment Name Address ID/FEI Business Operations Sun Deep Inc. 189788201 manufacture(61197-121)
