Amyl nitrosum

Manufacturer: Boiron | Boiron, Inc.
Effective date: 2024-03-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:26:24

Label at a glance#

ProductAmyl nitrosum

Active ingredientAMYL NITRITE

Label structure10 sections

Contacts and useful links#

PhoneLabel contact1-800-264-7661

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Amyl nitrosum 200CK HPUS

Active ingredient**: See product name on front panel (**contains 0.443 mg of the active ingredient per pellet).

INDICATIONS & USAGE SECTION

Uses: See symptoms on front panel.

Relieves hot flash followed by cold sweats *

OTC - STOP USE SECTION

Stop use and ask a doctor if symptoms persist for more than 3 days or worsen.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Adults and children: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.

INACTIVE INGREDIENT SECTION

lactose, sucrose

OTC - QUESTIONS SECTION

BoironUSA.com Info@boiron.com
1-800-BOIRON-1 (1-800-264-7661)
Distributed by Boiron, Inc.
Newtown Square, PA 19073

SPL UNCLASSIFIED SECTION

Do not use if pellet dispenser seal is broken.
Contains approx.80 pellets.
How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully remove the cap and use it to pour pellets under the tongue.
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
**C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0220-0302-41	Amyl nitrosum	200 [kp_C] in 1 TUBE	PELLET	200		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0220-0302	AMYL NITROSUM (AMYL NITRITE) PELLET [BOIRON]	1	Current NDC, 1 package rows	20240319_13f30f60-5157-6bab-e063-6294a90a6212.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Amyl nitrosum
AMYL NITRITE
LACTOSE, UNSPECIFIED FORM
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0220-0302	0220-0302-41

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
AMYL NITRITE	22T8Z09XAK	ACTIB
LACTOSE, UNSPECIFIED FORM	J2B2A4N98G	IACT
SUCROSE	C151H8M554	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Amyl nitrosum	AMYL NITRITE	Boiron	13f30f60-5157-6bab-e063-6294a90a6212	2024-03-18		Exact identifier ndc (package): 0220-0302-41 ndc (product): 0220-0302 ndc11 (package): 00220030241 spl id: 13f30f60-5158-6bab-e063-6294a90a6212 spl set id: 13f30f60-5157-6bab-e063-6294a90a6212

Reported adverse events (FAERS/openFDA)#

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