Calendula 10%

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.

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

"prepared using rhythmical processes"

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
shopuriel.com Lot#

Calendula 10

CALENDULA 10%
calendula 10% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-4165
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (CALENDULA OFFICINALIS FLOWERING TOP - UNII:18E7415PXQ)	CALENDULA OFFICINALIS FLOWERING TOP	1 [hp_X] in 1 g

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-4165-5	60 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/01/2009

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-4165)