GUNA-IL 10

GUNA-IL 10

Drug Labeling and Warnings

Drug Details

k">

GUNA-IL 10- interleukin-10 solution/ drops 
Guna spa

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.

----------

GUNA-IL 10

ACTIVE INGREDIENTS/PURPOSE

INTERLEUKIN-10    4C    CHRONIC PAIN RELIEF

USES

CHRONIC PAIN RELIEF

WARNINGS

Stop use and ask doctor if symptoms worsen or persist more than 5 days.

If pregnant or breast-feeding ask a doctor professional before use.
Keep this and all medicines out of reach of children.
Contains ethyl alcohol 30%


PREGNANCY

If pregnant or breast-feeding ask a doctor before use.

WARNINGS

Keep this and all medicines out of reach of children.

DIRECTIONS


Adults and children 12 years and older 20 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow.

Children between 12 years and 6 years of age 10 drops twice a day in a little water. Hold in the mouth for about 30 seconds then swallow.

Children under 6 years 5 drops twice a day in a glass of water.


QUESTIONS

Questions?: [email protected]
Tel. (484) 223-3500

Directions: Take 15 minutes before meals.

Inactive ingredient: Ethyl alcohol 30%.

PRINCIPAL DISPLAY PANEL

guna il 10 rev 1-2015

GUNA-IL 10 
interleukin-10 solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 17089-388
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
INTERLEUKIN-10 (UNII: 9SC4O216V9) (INTERLEUKIN-10 - UNII:9SC4O216V9) INTERLEUKIN-104 [hp_C]  in 30 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M) 9 mL  in 30 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 17089-388-181 in 1 BOX05/26/2010
130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic06/17/2008
Labeler - Guna spa (430538264)
Establishment
NameAddressID/FEIBusiness Operations
Guna spa338587646manufacture(17089-388)

Revised: 12/2018
 
Guna spa


© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.