FDA.reportPublic FDA data

Melissa Chamomilla Special Order

Manufacturer
Uriel Pharmacy Inc.
Effective date
2019-01-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:31:16

Label at a glance#

ProductMelissa Chamomilla Special Order
Active ingredientSEPIA OFFICINALIS JUICE, LACHESIS MUTA VENOM, MELISSA OFFICINALIS, ACONITUM NAPELLUS, MATRICARIA CHAMOMILLA, KALANCHOE DAIGREMONTIANA LEAF
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR TOPICAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

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

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Bryophyllum (Life plant) 1X, Chamomilla (Chamomile) 1X, Melissa (Lemon balm) 1X, Sepia (Squid ink) 4X, Aconitum (Monkshood) 8X, Lachesis (Bushmaster venom) 10X

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Use: Temporary relief of hot flashes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

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.

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Melissa Chamomilla Special Order CreamMelissa Chamomilla Special Order Cream

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
48951-717948951-7179-5

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
SEPIA OFFICINALIS JUICEQDL83WN8C2ACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
WATER059QF0KO0RIACT
STEARIC ACID4ELV7Z65APIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
LAVENDER OILZBP1YXW0H8IACT
CETYL ALCOHOL936JST6JCNIACT
POLYOXYL 40 STEARATE13A4J4NH9IIACT
STEARYL ALCOHOL2KR89I4H1YIACT
XANTHAN GUMTTV12P4NEEIACT
SORBIC ACIDX045WJ989BIACT
TEA TREE OILVIF565UC2GIACT
FRANKINCENSE OIL67ZYA5T02KIACT
MYRRH OILH74221J5J4IACT
CITRUS PARADISI SEED12F08874Y7IACT
MELISSA OFFICINALISYF70189L0NACTIB
ACONITUM NAPELLUSU0NQ8555JDACTIB
MATRICARIA CHAMOMILLAG0R4UBI2ZZACTIB
KALANCHOE DAIGREMONTIANA LEAFL6X13JKL8OACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c77e2e00-0c86-7415-e053-2995a90a63228021f3d8-2742-306a-e053-2a91aa0a33352021-07-19WarningsExact identifier
spl set id: 8021f3d8-2742-306a-e053-2a91aa0a3335

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.