TILIA EUROPAEA- tilia x europaea flower pellet
Washington Homeopathic Products

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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Tilia europaea X

ACTIVE INGREDIENTS

TILIA EUROPAEA

USES

To relieve the symptoms of profuse sweat.

KEEP OUT OF REACH OF CHILDREN

Keep this and all medicines out of reach of children.

INDICATIONS

Indications:

TILIA EUROPAEA Profuse sweat

STOP USE AND ASK DOCTOR

If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

DIRECTIONS

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides. Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

INACTIVE INGREDIENTS

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

Enter section text The OTC potency range of TILIA EUROPAEA is 2x–30x, 1c–30c, 200c, 1m, 10m, 50m, and CM.

Availability is subject to change.

Label

All WHP single remedies are made to order; thus, the labels are printed on the same label stock as the orders are filled.

‘Bottle Size’ and ‘Potency’ vary on the label depending on customer choice.

Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1 ounce, 2 ounce, and 4 ounce.

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TILIA EUROPAEA
tilia x europaea flower pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:68428-680
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TILIA X EUROPAEA FLOWER (UNII: NHV2K1OUDH) (TILIA X EUROPAEA FLOWER - UNII:NHV2K1OUDH)	TILIA X EUROPAEA FLOWER	30 [hp_C]

Ingredient Name	Strength
Inactive Ingredients
SUCROSE (UNII: C151H8M554)
LACTOSE (UNII: J2B2A4N98G)

Product Characteristics
Color	white (white)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:68428-680-03	75 in 1 VIAL, GLASS; Type 0: Not a Combination Product	02/03/2010
2	NDC:68428-680-05	150 in 1 VIAL, GLASS; Type 0: Not a Combination Product	02/03/2010	12/30/2020
3	NDC:68428-680-11	300 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	02/03/2010	12/30/2020
4	NDC:68428-680-12	600 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	02/03/2010	12/30/2020
5	NDC:68428-680-06	1200 in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	02/03/2010	12/30/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		02/03/2010	04/27/2022

Labeler - Washington Homeopathic Products (084929389)

Name	Address	ID/FEI	Business Operations
Establishment
Washington Homeopathic Products		084929389	manufacture(68428-680)

Revised: 4/2022

Document Id: dda51646-61f8-375d-e053-2995a90a4b17

Set id: 93ed4d38-97a1-447f-9415-19abbe56fa42

Version: 4

Effective Time: 20220427

Washington Homeopathic Products