Search by Drug Name or NDC

NDC 71094-0003-01 Tinnistop 8; 6; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1 Details

Tinnistop 8; 6; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1

Tinnistop is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Peerless Homeopathic. The primary component is ANAMIRTA COCCULUS SEED; CAUSTICUM; CONIUM MACULATUM FLOWERING TOP.

Product Information

NDC	71094-0003
Product ID	71094-0003_d7408b5c-e843-4370-b4a4-5400ac93eb70
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Tinnistop
Proprietary Name Suffix	n/a
Non-Proprietary Name	Causticum, Conium Maculatum, Cocculus Indicus
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	8; 6; 6
Active Ingredient Units	[hp_X]/1; [hp_X]/1; [hp_X]/1
Substance Name	ANAMIRTA COCCULUS SEED; CAUSTICUM; CONIUM MACULATUM FLOWERING TOP
Labeler Name	Peerless Homeopathic
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	UNAPPROVED HOMEOPATHIC
Application Number	n/a
Listing Certified Through	2023-12-31

Package

Package Images

NDC 71094-0003-01 (71094000301)

Pricing Information	N/A
NDC Package Code	71094-0003-1
Billing NDC	71094000301
Package	100 TABLET in 1 BOTTLE (71094-0003-1)
Marketing Start Date	2020-04-27
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL b5626577-1e09-469b-858f-92b4837b9300 Details

ACTIVE INGREDIENTS:

0.0033% of Causticum 6X, Conium Maculatum 6X, Cocculus Indicus 8X.

USES:

For the temporary relief of ringing and humming in the ears, and dizziness and nausea.

WARNINGS:

Do not use if safety seal is broken or missing.

A physician should always be consulted to rule out serious causes.

If pregnant or breast feeding, ask a physician before use. If symptoms persist for more than 7 days, consult a physician.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

OTHER INFORMATION:

Active ingredients are prepared in accordance with the Homeopathic Pharmacopoeia of the United States (HPUS) and are non-toxic with no known side effects.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Dissolve 1 tablet under the tongue 3 times a day, as needed. Store in a cool dry place.

INDICATIONS:

For the temporary relief of ringing and humming in the ears, and dizziness and nausea.

INACTIVE INGREDIENTS:

Lactose, Magnesium Stearate, Microcrystalline Cellulose

QUESTIONS:

More information available at:

www.TinniStop.com

Quality manufactured for and distributed by:

Peerless Homeopathic

PO Box 285 Roseland, VA 22967

PACKAGE LABEL DISPLAY:

TINNISTOP

Tinnitus & Vertigo Relief

Ringing

Buzzing

Dizziness

Nausea

Homeopathic

100 Tablets

INGREDIENTS AND APPEARANCE

TINNISTOP

causticum, conium maculatum, cocculus indicus tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71094-0003
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CAUSTICUM (UNII: DD5FO1WKFU) (CAUSTICUM - UNII:DD5FO1WKFU)	CAUSTICUM	6 [hp_X]
CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (CONIUM MACULATUM FLOWERING TOP - UNII:Q28R5GF371)	CONIUM MACULATUM FLOWERING TOP	6 [hp_X]
ANAMIRTA COCCULUS SEED (UNII: 810258W28U) (ANAMIRTA COCCULUS SEED - UNII:810258W28U)	ANAMIRTA COCCULUS SEED	8 [hp_X]

Ingredient Name	Strength
Inactive Ingredients
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)

Product Characteristics
Color	white	Score	no score
Shape	ROUND (CONVEX)	Size	6mm
Flavor		Imprint Code	DIAMOND
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71094-0003-1	100 in 1 BOTTLE; Type 1: Convenience Kit of Co-Package	04/27/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		04/27/2020

Labeler - Peerless Homeopathic (032675012)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(71094-0003) , api manufacture(71094-0003) , label(71094-0003) , pack(71094-0003)

Revised: 4/2020

Document Id: d7408b5c-e843-4370-b4a4-5400ac93eb70

Set id: b5626577-1e09-469b-858f-92b4837b9300

Version: 1

Effective Time: 20200427