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 determined that this product is safe, effect and not misbranded for its intended use."

INDICATION

VERTIGO, DIARREA, 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 advice 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 - 173 pellets.

CAUTION: Federal law prohibits dispensing without prescription

OPIUM3X.jpg

OPIUM 
raw opium gum pellet
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:10191-1081
Route of AdministrationSUBLINGUALDEA ScheduleCII    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OPIUM (UNII: 37M3MZ001L) (OPIUM - UNII:37M3MZ001L) OPIUM3 [hp_X]
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
LACTOSE (UNII: J2B2A4N98G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10191-1081-2160 in 1 VIAL, GLASS; Type 0: Not a Combination Product05/21/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic05/21/2015
Labeler - Remedy Makers (018543582)

Revised: 3/2023
Document Id: f65aaf54-bcd1-50a9-e053-2995a90a9042
Set id: 196e58dc-6fb2-35bb-e054-00144ff88e88
Version: 8
Effective Time: 20230307
 
Remedy Makers