NASAL EASE ALLERGY RELIEVER- potassium dichromate powder
Health Care Products

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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Drug Facts

Active ingredient

Potassium Dichromate (Kall Bichromicum 3x)

Purpose

Sneezing, Sinus congestion, and Runny nose

Keep Out of Reach of Children

Uses

Temporary relieves three symptoms of hay fever and allergic rhinitis;

Sneezing;

Sinus congestion;

Runny nose;

Warnings

For nasal use only.

Stop use and ask a doctor

if symptoms do not improve within 7 days or are accompanied by fever.

Do Not Use

in children under 12 years of age.

If pregnant or breast-feeding

consult a doctor.

Keep Out of Reach of Children

Directions

Adults and Children over 12 ........ 1-2 doses daily

Children under 12 ........ Consult a doctor

Gently blow your nose. While breathing normally, place tip of dispenser just inside the nostril and firmly squeeze the bottle to distribute powder. Repeat in other nostril. Once opened, use within 6 months. Do not use if tamper evident seal on bottle is broken or missing. Store in a cool dry place.

Inactive Ingredients

Cellulose

Package/Label Principal Display Panel

NDC 61787-482-50

Nasel Ease

Homeopathic

ALLERGY RELIEVER

NEW!

Relieves

SNEEZING
SINUS CONGESTION
RUNNY NOSE

Net weight 0.18 oz

200 Doses

Nasal Powder Spray

NASAL EASE ALLERGY RELIEVER
potassium dichromate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:61787-482
Route of Administration	NASAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POTASSIUM DICHROMATE (UNII: T4423S18FM) (DICHROMATE ION - UNII:9LKY4BFN2V)	POTASSIUM DICHROMATE	200 [AU] in 5.1 g

Ingredient Name	Strength
Inactive Ingredients
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:61787-482-50	1 in 1 BOX	08/03/2009	10/31/2015
1		5.10 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
Unapproved homeopathic		08/03/2009	10/31/2015

Labeler - Health Care Products (101196749)

Registrant - Hi-Tech Pharmacal Co., Inc. (101196749)

Name	Address	ID/FEI	Business Operations
Establishment
Nasaleze LTD		233326748	MANUFACTURE(61787-482)

Revised: 12/2018

Document Id: 658ab2c3-ac7d-47c7-9dea-e1ef75f5c08b

Set id: 8e61d498-8697-44be-93b0-feedaead9ae3

Version: 2

Effective Time: 20181204

Health Care Products