GUNA-TF HERPES- human herpesvirus 1 - human herpesvirus 2 - capsule, gelatin coated

GUNA-TF HERPES by

Drug Labeling and Warnings

GUNA-TF HERPES by is a Homeopathic medication manufactured, distributed, or labeled by Guna spa. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS/PURPOSE

TRANSFER FACTOR HV1    7X    IMMUNE STRENGTHENING
TRANSFER FACTOR HV2    7X    IMMUNE STRENGTHENING

USES

For the temporary relief of symptoms due to cold sores: pain, tingling, burning sensation.

WARNINGS

Stop use and ask doctor if symptoms of tingling or burning sensation worsen or persist more than 5 days

PREGNANCY

If pregnant or breast-feeding ask a doctor before use

WARNINGS

Keep this and all medicines out of reach of children

DIRECTIONS

Take 15 minutes before meals
Adults and children 12 years and older    1 capsule per day with a little water
Children  between 12 years and 6 years of age    1 capsule every other day, with a little water
Children under 6 years     1 capsule every other day. Open the capsule and place the content on a spoon with a little water

QUESTIONS

Questions?: info@gunainc.com
Tel. (484) 223-3500

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GUNA-TF HERPES 
human herpesvirus 1 - human herpesvirus 2 - capsule, gelatin coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17089-269
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL) (HUMAN HERPESVIRUS 1 - UNII:22G38P19RL)	HUMAN HERPESVIRUS 1	7 [hp_X]  in 4600 mg
HUMAN HERPESVIRUS 2 (UNII: 74J6DNH49U) (HUMAN HERPESVIRUS 2 - UNII:74J6DNH49U)	HUMAN HERPESVIRUS 2	7 [hp_X]  in 4600 mg

Inactive Ingredients
Ingredient Name	Strength
LACTOSE (UNII: J2B2A4N98G)	4048 mg  in 4600 mg
MAGNESIUM STEARATE (UNII: 70097M6I30)	92 mg  in 4600 mg

Product Characteristics
Color	white (white)	Score	2 pieces
Shape	OVAL (Capsule)	Size	18mm
Flavor		Imprint Code	na
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17089-269-10	1 in 1 BOX
1		4600 mg in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		05/23/2006

Labeler - Guna spa (430538264)

Establishment
Name	Address	ID/FEI	Business Operations
Guna spa		430538264	manufacture