WAXUP NUMBING- lidocaine hydrochloride liquid 
CONSTRUSOLUTION, LLC

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WAXUP Numbing Spray

Drug Facts

Active Ingredients

Lidocaine HCL 5.00%

Purpose

Anorectal (hemorrhoidal)

Uses:

Warnings:

For external use only.

Do not:

  • exceed the recommended daily dosage unless directed by a doctor.
  • put this product into the rectum by using fingers or any mechanical device or applicator.

When using this product:

  • If condition worsens or does not improve within 7 days, consult a doctor.
  • In case of bleeding, consult a doctor promptly.

Stop use and ask a doctor if:

  • If the symptom being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase.
  • Certain persons can develop allergic reactions to ingredients in this product.

Allergy alert: 

Keep out of raech of children.

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

If pregnant or breast-feeding, 

ask a health professional before use.

Directions:

Adults:• When practical, cleanse the affected area "with mild soap and warm water and rinse by patting or blotting with an appropriate cleansing pad. • Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. • Children under 12 years of age: consult a doctor. • Apply externally to the affected area up to 6 times daily or after each bowel movement.

Other Information:

Inactive ingredients:

Allantoin, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Benzyl Alcohol, Carbomer, Ethylhexylglycerin, Phenoxyethanol, Propylene Glycol, Tetrasodium EDTA, Tocopheryl Acetate (Vitamin E), Triethanolamine, Zemea (Corn) Propanediol.

Package Labeling:

Label

WAXUP NUMBING 
lidocaine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83163-386
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALLANTOIN (UNII: 344S277G0Z)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
EDETATE SODIUM (UNII: MP1J8420LU)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TROLAMINE (UNII: 9O3K93S3TK)  
CORN (UNII: 0N8672707O)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83163-386-001 in 1 BOX12/23/2022
159.14 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01512/23/2022
Labeler - CONSTRUSOLUTION, LLC (054145965)

Revised: 11/2023
Document Id: 0976ef49-eccc-1b67-e063-6294a90a4ec6
Set id: 4f1645ab-1b19-4d69-99c3-9ea275b01a87
Version: 2
Effective Time: 20231106
 
CONSTRUSOLUTION, LLC