MELISSA CHAMOMILLA- melissa chamomilla liquid
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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Melissa Chamomilla

Directions: FOR ORAL USE ONLY.

Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.

Active Ingredients: Bryophyllum e fol. 3X, Chamomilla e rad. 3X, Melissa ex herba 3X, Sepia e secreto 6X, Aconitum e tub. 10X, Lachesis e veneno 12X

Inactive Ingredients: Water, Salt

Use: Temporary relief of hot flashes.

KEEP OUT OF REACH OF CHILDREN.

Warnings: 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 or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.

Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 shopuriel.com

Melissa Chamomilla Ampules

MELISSA CHAMOMILLA
melissa chamomilla liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:48951-7027
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
MELISSA OFFICINALIS (UNII: YF70189L0N) (MELISSA OFFICINALIS - UNII:YF70189L0N)	MELISSA OFFICINALIS	3 [hp_X] in 1 mL
SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2)	SEPIA OFFICINALIS JUICE	6 [hp_X] in 1 mL
ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD)	ACONITUM NAPELLUS	10 [hp_X] in 1 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	12 [hp_X] in 1 mL
KALANCHOE DAIGREMONTIANA LEAF (UNII: L6X13JKL8O) (KALANCHOE DAIGREMONTIANA LEAF - UNII:L6X13JKL8O)	KALANCHOE DAIGREMONTIANA LEAF	3 [hp_X] in 1 mL
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ) (MATRICARIA RECUTITA - UNII:G0R4UBI2ZZ)	MATRICARIA RECUTITA	3 [hp_X] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:48951-7027-1	10 in 1 BOX	09/01/2009	01/01/2024
1		1 mL in 1 AMPULE; Type 1: Convenience Kit of Co-Package

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		09/01/2009	01/01/2024

Labeler - Uriel Pharmacy Inc. (043471163)

Name	Address	ID/FEI	Business Operations
Establishment
Uriel Pharmacy Inc.		043471163	manufacture(48951-7027)

Revised: 1/2024

Document Id: 0f2816f0-b5a3-6927-e063-6394a90a8287

Set id: 2d5b8cba-439a-48fd-a261-be59f126974e

Version: 4

Effective Time: 20240117

Uriel Pharmacy Inc.