DRXNOZE NOSEBLEED RELIEF- achillea millefolium, marrubium vulgare, stachys betonica, urtica dioica swab

DrxNoze Nosebleed Relief by

Drug Labeling and Warnings

DrxNoze Nosebleed Relief by is a Homeopathic medication manufactured, distributed, or labeled by ByzMed, LLC, Oasis Health Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Achillea millefolium 1X, Marrubium vulgare 1X, Stachys betonica 1X, Urtica dioica 1X

Purpose

Astringent

Keep Out of Reach of Children

Keep out of the reach of children.

Uses

Shortens duration of minor nose bleeds.

Warnings

For Nasal Passage Use Only. Do not use if you are allergic to any ingredient in this product.

When using this product

• Avoid contact with eyes.
• Do not use for deep or puncture wounds, animal bites, or serious burns.
• In case of accidental contact with eyes, flush with water and immediately seek professional help.
• Keep out of the reach of children.
• Each applicator is designed for one person, single use.
• If pregnant or breastfeeding, ask a health professional before use.
• Consult a physician if bleeding persists for longer than 30 minutes.
• Consult a physician if symptoms persist for more than 7 days or worsen.
• Do not use if seal is broken.
• Children under 6 years of age: consult a physician before use.
• In case of overdose, get medical help or contact a Poison Control Center immediately.

Directions

Adults and children 6 years and older:
1. Peel back tab on package to expose swab.
2. Remove swab from package.
3. Blow nose gently to remove excess blood from nasal passage.
4. Apply swab to affected area in nasal passage.
5. Pinch nostril with swab in place (tilt chin slightly downward).
6. Keep swab in place for 1 minute.
7. Remove swab and gently blow out excess blood from nostril.
8. If bleeding persists, twist swab ½ turn and reinsert for 1-2 minutes or until bleeding stops.
9. Dispose of swab after use.

Inactive Ingredients

aloe vera, citric acid, glycerin, hydroxyethyl-cellulose, polysorbate 20, potassium sorbate, purified water, sodium benzoate, sodium chloride

Other Information

Store at 68-77°F (20-25°C)

Package/Label Principal Display Panel

DRxNOZE® NOSEBLEED RELIEF

Works Fast! Natural Active Ingredients!

• Helps natural blood clotting
• Easy to use, works quickly
• No stinging
• Effective stopping rebleeds
• No strips to clog nostrils
• Pharmacist developed

Contains 5 Nasal Swabs (1 swab per dose)

Homeopathic

Manufactured and distributed for:

ByzMed, LLC

Cottage Grove, WI 53527 USA

www.DrxNoze.com

Made in the USA

US Patent 8,414,935

Foreign application pending

©2013 Byzmed, LLC

Questions or comments? Call (866-473-1740) or email us at: customerservice@DrxNoze.com.

Visit us at www.DrxNoze.com

These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Carton Label – Front

•   Carton Label – Back

INGREDIENTS AND APPEARANCE

DRXNOZE NOSEBLEED RELIEF 
achillea millefolium, marrubium vulgare, stachys betonica, urtica dioica swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58092-001
Route of Administration	NASAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (ACHILLEA MILLEFOLIUM - UNII:2FXJ6SW4PK)	ACHILLEA MILLEFOLIUM	1 [hp_X]  in 1.5 mL
MARRUBIUM VULGARE (UNII: 7A72MUN24Z) (MARRUBIUM VULGARE - UNII:7A72MUN24Z)	MARRUBIUM VULGARE	1 [hp_X]  in 1.5 mL
STACHYS OFFICINALIS (UNII: UO9989Y17N) (STACHYS OFFICINALIS - UNII:UO9989Y17N)	STACHYS OFFICINALIS	1 [hp_X]  in 1.5 mL
URTICA DIOICA (UNII: 710FLW4U46) (URTICA DIOICA - UNII:710FLW4U46)	URTICA DIOICA	1 [hp_X]  in 1.5 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58092-001-01	5 in 1 CARTON
1		1.5 mL in 1 BLISTER PACK

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved homeopathic		02/01/2014

Labeler - ByzMed, LLC (828557921)

Registrant - Oasis Health Products, Inc. (964858315)