CLEAR ITCH RELIEF EVORA LABS- pramoxine hcl, zinc acetate spray 
Evora Worldwide

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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Drug Facts

Active ingredients                               Purpose

Pramoxine HCl                                    Topical analgesic

Zinc Acetate                                        Skin protectant

Uses

• Temporanly relieves pain and itching associated with:

rashes due to poison ivy, poison oak or poison sumac
insect bites
minor skin irritation
minor cuts
dries the oozing and weeping of poison ivy, poison oak and poison sumac

Warnings
For external use only

Flammable: Do not use while smoking or near heat or flame
Stop use and ask doctor if • condition worsens or does not improve within 7 days • symptoms persist for more than 7 days or clear up and
occur again with 1n a few days

When using this product keep out of eyes. Rinse with water to remove. Do not puncture or incinerate. Contents are under pressure. Do not store at temparatures above 1200F.

Keep out or reach or children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

• shake well before use • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily• children under 2 years of age: ask a doctor

Inactive inaredients

Avena sativa (OatMeal) Extract, Camphor, Citric Acid, Diazolidinyl Urea, Fragrance, Glycerin, Hydroxypropyl Methylcellulose, Methylparaben,
Polysorbate 40, Propylene Glycol, Propylparaben, SD Alcohol 38-B, Sodium Citrate, Water

Questions?

1-888-793-8450

image description

CLEAR ITCH RELIEF  EVORA LABS
pramoxine hcl, zinc acetate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77375-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE1 g  in 100 g
ZINC ACETATE (UNII: FM5526K07A) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION0.1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
OATMEAL (UNII: 8PI54V663Y)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYSORBATE 40 (UNII: STI11B5A2X)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
ALCOHOL (UNII: 3K9958V90M)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:77375-004-0285 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/01/202012/31/2020
Labeler - Evora Worldwide (081336028)
Establishment
NameAddressID/FEIBusiness Operations
Inspec Solutions LLC081030372manufacture(77375-004)

Revised: 12/2020
 
Evora Worldwide