RHUS TOX. 1 SPECIAL ORDER- rhus tox. 1 special order cream
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.

----------

Rhus tox. 1 Special Order

Directions: FOR TOPICAL USE ONLY.

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

Active Ingredient: Rhus tox. (Sumac) 2X

Inactive Ingredients: Distilled water, Stearic acid, Isopropyl myristate, Lavender oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Potassium sorbate, Frankincense oil, Myrrh oil, Grapefruit seed extract

Use: Temporary relief of rash.

KEEP OUT OF REACH OF CHILDREN.

Warnings: FOR EXTERNAL USE ONLY. 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

rhutox1crmSO

RHUS TOX. 1 SPECIAL ORDER
rhus tox. 1 special order cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-8242
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	2 [hp_X] in 1 g

Ingredient Name	Strength
Inactive Ingredients
MYRRH OIL (UNII: H74221J5J4)
CITRUS PARADISI SEED (UNII: 12F08874Y7)
WATER (UNII: 059QF0KO0R)
STEARIC ACID (UNII: 4ELV7Z65AP)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
LAVENDER OIL (UNII: ZBP1YXW0H8)
CETYL ALCOHOL (UNII: 936JST6JCN)
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
XANTHAN GUM (UNII: TTV12P4NEE)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
FRANKINCENSE OIL (UNII: 67ZYA5T02K)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-8242-5	60 g in 1 TUBE; Type 0: Not a Combination Product	09/01/2009	10/09/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/01/2009	10/09/2020

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-8242)

Revised: 6/2021

Document Id: c574a559-b966-fa50-e053-2995a90a723e

Set id: 2c6840d3-ada8-425c-8f39-fd58be707234

Version: 3

Effective Time: 20210623

Uriel Pharmacy Inc.