OPIUM- raw opium gum pellet 
Remedy Makers

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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CII

WARNING:

"The FDA has not deternined that this product is safe, effective and not misbranded for its intended use".

INDICATION:

VERTIGO, DIARRHEA, PAIN OR OTHER INDICATIONS

WARNING:

Use only if cap and seal are unbroken. Keep this and all medication out of reach of children. If symptoms persist more than 3 days or worsen, discontinue (STOP) use and consult your physician. As with any drug. If you are pregnant or nursing (breast-feeding) a baby, seek the advise of a health professional before using this product. Store tightly closed in a cool area.

Directions (adult/children)

Dissolve 3 or 4 pellets in mouth under tongue 3 times a day or as directed by a physician. Children 2 years and older take 1/2 adult dose.

Inactive Ingredients:

Lactose and Sucrose. Free from yeast, wheat, corn, and soy.

Questions or comments:

(877)REM4YOU Fax (909) 594-4205 Pomona, CA. 91768 USA www.remedymakers.com

Other Information:

Contains approx. 160 - 164 pellets.

CAUTION:

Federal law prohibits dispensing without prescription.

OPIUM6X

OPIUM 
raw opium gum pellet
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:10191-1082
Route of AdministrationSUBLINGUALDEA ScheduleCII    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OPIUM (UNII: 37M3MZ001L) (OPIUM - UNII:37M3MZ001L) OPIUM6 [hp_X]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
LACTOSE (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10191-1082-2160 in 1 VIAL, GLASS; Type 0: Not a Combination Product07/07/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic07/06/2015
Labeler - Remedy Makers (018543582)

Revised: 3/2023
Document Id: f65aadda-613e-669f-e053-2a95a90a817a
Set id: 19eb9717-94a0-2fd5-e054-00144ff8d46c
Version: 2
Effective Time: 20230307
 
Remedy Makers