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NDC 72968-0004-01 Herplex 12; 12; 12; 12; 12; 30; 30; 12; 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 Details

Herplex 12; 12; 12; 12; 12; 30; 30; 12; 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1

Herplex is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Nashco Products LLC. The primary component is CHRYSOPOGON ZIZANIOIDES ROOT; CLEMATIS RECTA FLOWERING TOP; DAPHNE MEZEREUM BARK; PHYTOLACCA AMERICANA ROOT; RANUNCULUS BULBOSUS WHOLE; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF.

Product Information

NDC	72968-0004
Product ID	72968-0004_1d44a27d-7870-4a51-88ec-195c547bbad0
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	Herplex
Proprietary Name Suffix	n/a
Non-Proprietary Name	Anatherum Muricatum, Clematis Erecta, Mezereum, Phytolacca Decandra, Ranunculus Bulbosus, Rhus Tox, Thuja Occidentalis, Natrum Muriaticum, Sepia
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	12; 12; 12; 12; 12; 30; 30; 12; 12
Active Ingredient Units	[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Substance Name	CHRYSOPOGON ZIZANIOIDES ROOT; CLEMATIS RECTA FLOWERING TOP; DAPHNE MEZEREUM BARK; PHYTOLACCA AMERICANA ROOT; RANUNCULUS BULBOSUS WHOLE; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF
Labeler Name	Nashco Products LLC
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	UNAPPROVED HOMEOPATHIC
Application Number	n/a
Listing Certified Through	2024-12-31

Package

Package Images

NDC 72968-0004-01 (72968000401)

Pricing Information	N/A
NDC Package Code	72968-0004-1
Billing NDC	72968000401
Package	120 TABLET in 1 BOTTLE, PLASTIC (72968-0004-1)
Marketing Start Date	2022-08-30
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 6a1322c7-7767-4569-aa22-9d2e36331283 Details

ACTIVE INGREDIENTS:

Anatherum Muricatum 12X, Clematis Erecta 12X, Mezereum 12X, Phytolacca Decandra 12X, Ranunculus Bulbosus 12X, Rhus Tox 12X, Thuja Occidentalis 12X, Sepia 30X, Natrum Muriaticum 30X.

USES:

Herplex can be used to temporarily relieve pain and itching during outbreads of cold sores and fever blisters.

WARNINGS:

CAUTION: Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Not recommended for children under 12.

If you are pregnant or breast-feeding, ask your doctor before use.

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SHRINK SEAL AROUND NECK AND CAP IS BROKEN OR MISSING.

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:

For use only after diagnoses by a physician, as follows:

Cold Sores/Fever Blisters For mild to moderate symptoms, take 3 tablets immediately at the first sign of burning or itching, and then 3 tablets three times daily until symptoms subside. For sufferers of severe outbreaks, take 3 to 5 tablets 3 times daily to help prevent or reduce outbreaks. If you have an outbreak that does not subside within 10 days, consult your doctor.

USES:

Herplex can be used for temporarily relieve pain and itching during outbreads of cold sores and fever blisters.

INACTIVE INGREDIENTS:

Lactose, Magnesium Stearate, Microcrystalline Cellulose.

QUESTIONS:

DISTRIBUTED BY: Nashco Products LLC

131 Daniel Webster Highway #957

Nashua, NH 03060

603-215-7855

Questions or comments?

Visit us at www.BuyHerplex.com

PACKAGE LABEL DISPLAY:

COLD SORES/FEVER BLISTERS

Herplex

A New Beginning

•Safe •Non-prescription

•Homeopathic

120 TABLETS

INGREDIENTS AND APPEARANCE

HERPLEX

anatherum muricatum, clematis erecta, mezereum, phytolacca decandra, ranunculus bulbosus, rhus tox, thuja occidentalis, natrum muriaticum, sepia tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:72968-0004
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHRYSOPOGON ZIZANIOIDES ROOT (UNII: 37TB8LUP9Z) (CHRYSOPOGON ZIZANIOIDES ROOT - UNII:37TB8LUP9Z)	CHRYSOPOGON ZIZANIOIDES ROOT	12 [hp_X]
CLEMATIS RECTA FLOWERING TOP (UNII: 396421SP9F) (CLEMATIS RECTA FLOWERING TOP - UNII:396421SP9F)	CLEMATIS RECTA FLOWERING TOP	12 [hp_X]
DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (DAPHNE MEZEREUM BARK - UNII:X2N6E405GV)	DAPHNE MEZEREUM BARK	12 [hp_X]
PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (PHYTOLACCA AMERICANA ROOT - UNII:11E6VI8VEG)	PHYTOLACCA AMERICANA ROOT	12 [hp_X]
RANUNCULUS BULBOSUS WHOLE (UNII: AEQ8NXJ0MB) (RANUNCULUS BULBOSUS - UNII:AEQ8NXJ0MB)	RANUNCULUS BULBOSUS WHOLE	12 [hp_X]
TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A)	TOXICODENDRON PUBESCENS LEAF	12 [hp_X]
THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397)	THUJA OCCIDENTALIS LEAFY TWIG	12 [hp_X]
SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (SEPIA OFFICINALIS JUICE - UNII:QDL83WN8C2)	SEPIA OFFICINALIS JUICE	30 [hp_X]
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	30 [hp_X]

Ingredient Name	Strength
Inactive Ingredients
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM PALMITOSTEARATE (UNII: R4OXA9G5BV)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	H
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72968-0004-1	120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/30/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		08/30/2022

Labeler - Nashco Products LLC (116986692)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(72968-0004) , api manufacture(72968-0004) , label(72968-0004) , pack(72968-0004)

Revised: 8/2022

Document Id: 1d44a27d-7870-4a51-88ec-195c547bbad0

Set id: 6a1322c7-7767-4569-aa22-9d2e36331283

Version: 1

Effective Time: 20220830

Search by Drug Name or NDC

NDC 72968-0004-01 Herplex 12; 12; 12; 12; 12; 30; 30; 12; 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 Details

Herplex 12; 12; 12; 12; 12; 30; 30; 12; 12 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1

Product Information

Package

Package Images

NDC 72968-0004-01 (72968000401)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 6a1322c7-7767-4569-aa22-9d2e36331283 Details

ACTIVE INGREDIENTS:

USES:

WARNINGS:

KEEP OUT OF REACH OF CHILDREN:

DIRECTIONS:

USES:

INACTIVE INGREDIENTS:

QUESTIONS:

PACKAGE LABEL DISPLAY:

INGREDIENTS AND APPEARANCE

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