CALENDULA 10%- calendula 10% gel 
Uriel Pharmacy Inc.

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.

----------

Calendula 10%

Directions: FOR TOPICAL USE ONLY.

Apply to skin as needed. Under age 2: Consult a doctor.

Active Ingredient: 100 gm contains: 50 gm Calendula 1X

Inactive Ingredients: Distilled water, Organic cane alcohol, Glycerin, Boric acid, Sodium alginate,
Lavender oil, Sodium hydroxide, Sorbic acid, Tea tree oil, Grapefruit seed extract

Uses: Temporary relief of minor cuts and wounds.

KEEP OUT OF REACH OF CHILDREN.

Warnings: FOR EXTERNAL USE ONLY.
Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist,
or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes.
Do not use if safety seal is broken or missing.

Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
www.urielpharmacy.com Lot#

Calendula 10 Gel

CALENDULA 10% 
calendula 10% gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-4165
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ) CALENDULA OFFICINALIS FLOWERING TOP1 [hp_X]  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM ALGINATE (UNII: C269C4G2ZQ)  
SORBIC ACID (UNII: X045WJ989B)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
TEA TREE OIL (UNII: VIF565UC2G)  
CITRUS PARADISI SEED (UNII: 12F08874Y7)  
BORIC ACID (UNII: R57ZHV85D4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:48951-4165-560 g in 1 TUBE; Type 0: Not a Combination Product09/01/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/01/2009
Labeler - Uriel Pharmacy Inc. (043471163)
Establishment
NameAddressID/FEIBusiness Operations
Uriel Pharmacy Inc.043471163manufacture(48951-4165)

Revised: 5/2021
Document Id: c19b1db8-df52-e8fc-e053-2a95a90aee03
Set id: c19b1db8-df51-e8fc-e053-2a95a90aee03
Version: 1
Effective Time: 20210505
 
Uriel Pharmacy Inc.