NATUREPLEX PSORIASIS- salicylic acid cream 
Natureplex LLC

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.

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NATUREPLEX™ PSORIASIS

Drug Facts

Active ingredient

Salicylic acid 2%

Purpose

Psoriasis and seborrheic dermatitis

Uses

Reduces and helps prevent recurrence of

Warnings

For external use only.

Ask a doctor before use if condition covers a large area of the body

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if condition worsens or does not improve after regular use.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.

Directions

Apply to affected areas one to four times daily or as directed by a doctor.

Other information

Inactive ingredients

alcohol denatured, caprylic/capric triglyceride, carbomer, cetyl alcohol, DMDM hydantoin, glyceryl stearate, methylparaben, mineral oil, polysorbate-20, propylene glycol, propylparaben, purified water, stearic acid, triethanolamine, trisodium EDTA, vitamin A (as retinyl palmitate), vitamin D (as cholecalciferol)

Questions or comments?

866-323-0107 or www.natureplex.com

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton

Natureplex™
PSORIASIS
Medicated Moisturizer

NET WT. 1 Oz. (28g)

NDC 67234-073-01

Salicylic
Acid 2%

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton
NATUREPLEX PSORIASIS 
salicylic acid cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67234-073
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MINERAL OIL (UNII: T5L8T28FGP)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TROLAMINE (UNII: 9O3K93S3TK)  
EDETATE TRISODIUM (UNII: 420IP921MB)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67234-073-011 in 1 CARTON07/24/2019
128 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H07/24/2019
Labeler - Natureplex LLC (062808196)
Establishment
NameAddressID/FEIBusiness Operations
Natureplex LLC062808196MANUFACTURE(67234-073)

Revised: 1/2021
Document Id: 81626372-eadb-4544-9222-855eb6dea9df
Set id: 1efa3e8d-f80b-44f4-a233-187e3329dd8f
Version: 2
Effective Time: 20210112
 
Natureplex LLC