NATRALIA ACNE WASH- silicon dioxide and sodium chloride liquid 
LaCorium Health International Pty Ltd

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.

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natralia™
NATURALLY AUSTRALIAN

acne wash

Drug Facts

Active ingredientsPurpose
*
The letters H.P.U.S. indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.
Silica (3× HPUS 0.05%)*Acne Control
Natrum Muriaticum (12× HPUS 0.05%)*Acne Control

Uses

Warnings

  • If condition worsens or does not improve after regular use of this product as directed or if local irritation or rash occurs, discontinue use and consult a physician

  • Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water

  • Keep out of reach of children

Directions

Other information

Store between 50°- 86°F.

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

Questions or comments?

Call Toll Free 1-877- 687-2542

PRINCIPAL DISPLAY PANEL - 200mL Tube Label

natralia™
NATURALLY AUSTRALIAN

acne wash

natural homeopathic alternative

Cleanse & Exfoliate

Contains 0.025% ethanol w/w

7 fl oz (200mL)

598FLA-3

PRINCIPAL DISPLAY PANEL - 200mL Tube Label
NATRALIA  ACNE WASH
silicon dioxide and sodium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43251-3323
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE3 [hp_X]  in 1 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE12 [hp_X]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:43251-3323-5200 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved homeopathic03/01/2009
Labeler - LaCorium Health International Pty Ltd (758651624)
Establishment
NameAddressID/FEIBusiness Operations
Jalco Pharmaceuticals Pty Ltd757701409MANUFACTURE(43251-3323) , PACK(43251-3323) , LABEL(43251-3323) , ANALYSIS(43251-3323)

Revised: 12/2012
Document Id: 134b3385-4249-41ba-98b8-f800cf994114
Set id: f965b14a-f060-472d-842e-5b497cc1e0c1
Version: 3
Effective Time: 20121219
 
LaCorium Health International Pty Ltd