AMBRA GRISEA- ambergris pellet 
Boiron

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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Ambra grisea

Ambra grisea

6C,12C,15C,30C,200CK

Ocassional sleeplessness with hypersensitivity*

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

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

Keep out of reach of children

5 pellets 3 times a day until symptoms are relieved

Do not use if pellet dispenser seal is broken

contains approx 80 pellets

lactose, sucrose

1-800-BOIRON-1

Newtown Square, PA 19073-3267

info@boironusa.com

These "Uses" have not been evaluated by the FDA

labellabel

AMBRA GRISEA 
ambergris pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0220-0221
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AMBERGRIS (UNII: XTC0D02P6C) (AMBERGRIS - UNII:XTC0D02P6C) AMBERGRIS6 [hp_C]  in 6 [hp_C]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
Product Characteristics
ColorwhiteScore    
ShapeROUNDSize4mm
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0220-0221-416 [hp_C] in 1 TUBE; Type 0: Not a Combination Product03/03/198309/13/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic03/03/198309/13/2018
Labeler - Boiron (282560473)
Registrant - Boiron, Inc. (014892269)
Establishment
NameAddressID/FEIBusiness Operations
Boiron282560473manufacture(0220-0221)
Establishment
NameAddressID/FEIBusiness Operations
Boiron380022322manufacture(0220-0221)

Revised: 7/2020
 
Boiron