Base Laboratories Hemorrhoidal Cream

Base Laboratories Hemorrhoidal by

Drug Labeling and Warnings

Base Laboratories Hemorrhoidal by is a Otc medication manufactured, distributed, or labeled by Joonem LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BASE LABORATORIES HEMORRHOIDAL- lidocaine cream 
Joonem LLC

----------

Base Laboratories Hemorrhoidal Cream

Drug Facts

Active ingredients

Lidocaine 5%

Purpose

Topical Analgesic

Indications

For the temporary relief of anorectal discomfort, itching, pain, soreness  associated with hemorrhoids, anorectal disorders or inflamed hemorrhoidal tissues

Warnings:

If condition worsens or does not improve within 7 days, consult a doctor.

  • Do not exceed the recommended daily dosage unless directed by a doctor.
  • In case of bleeding, consult a doctor promptly.
  • Do not put this product into the rectum by using fingers or any mechanical device or applicator.
  • Certain persons can develop allergic reactions to ingredients in this product. If symptoms being treated does not subside or if redness, irritation, swelling, pain, or other symptoms develop or increases, discontinue use and consult a doctor.

Keep out of reach of children to avoid accidental ingestion!

If swallowed, get medical help or contact a poison control center immediately.

Directions

  • Adults: When practical, cleanse the affected area with mild soap and warm water and rinse thoroughly or 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. Apply externally to the affected area up to 6 timess daily. 
  • Children under 12 years of age:
  • consult a doctor.  

Inactive Ingredients

Aloe Vera, Calendula Oil, Bhringraja Oil, Hemp Seed Oil, Zinc Oxide, Glycerin, Phenylephrine Hydrchloride, Carbopol 940, Cetostearyl Alcohol, Cetyl Alcohol, Cetearyl Alcohol, Cetyl Palmitate, Cetomacrogol 1000, Silicon Oil 350, Propylene glycol, Triethanolamine,  Phenoxyethanol, Ethylhexylglycerin, DM Water

Package Label

image description

BASE LABORATORIES HEMORRHOIDAL 
lidocaine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 80327-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)  
CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
CETYL PALMITATE (UNII: 5ZA2S6B08X)  
CETETH-20 (UNII: I835H2IHHX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TROLAMINE (UNII: 9O3K93S3TK)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 80327-005-01120 mL in 1 TUBE; Type 0: Not a Combination Product09/01/202003/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01509/01/202003/31/2022
Labeler - Joonem LLC (117633878)

Revised: 1/2024

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.