Label: NATRALIA ACNE WASH- silicon dioxide and sodium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 43251-3323-5 - Packager: LaCorium Health International Pty Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated December 19, 2012
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Inactive ingredients
Aloe Vera Gel, Benzyl Alcohol, Calendula Officinalis (Calendula) Extract, Caprylyl Glycol (and) Sorbic Acid (and) Phenoxyethanol, Cocoamidopropyl Betaine, Disodium Cocoamphodiacetate, Hamamelis Virginiana (Witch Hazel) Distillate, Lactic Acid, Lauryl Glucoside, Lavandula Angustifolia (Lavender) Oil, Melaleuca Alternifolia (Tea Tree) Oil, Palmarosa Essential Oil, PEG-150 Distearate, Polysorbate 20, Water
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- PRINCIPAL DISPLAY PANEL - 200mL Tube Label
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INGREDIENTS AND APPEARANCE
NATRALIA ACNE WASH
silicon dioxide and sodium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43251-3323 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 3 [hp_X] in 1 mL SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 12 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) BENZYL ALCOHOL (UNII: LKG8494WBH) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) LACTIC ACID (UNII: 33X04XA5AT) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SORBIC ACID (UNII: X045WJ989B) PHENOXYETHANOL (UNII: HIE492ZZ3T) PALMAROSA OIL (UNII: 0J3G3O53ST) PEG-150 DISTEARATE (UNII: 6F36Q0I0AC) POLYSORBATE 20 (UNII: 7T1F30V5YH) TEA TREE OIL (UNII: VIF565UC2G) WITCH HAZEL (UNII: 101I4J0U34) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43251-3323-5 200 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 03/01/2009 Labeler - LaCorium Health International Pty Ltd (758651624) Establishment Name Address ID/FEI Business Operations Jalco Pharmaceuticals Pty Ltd 757701409 MANUFACTURE(43251-3323) , PACK(43251-3323) , LABEL(43251-3323) , ANALYSIS(43251-3323)