NDC 61657-0327 Hpz

NDC Product Code 61657-0327

NDC 61657-0327-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Hpz with NDC 61657-0327 is a product labeled by White Manufacturing Inc. Dba Micro-west. The generic name of Hpz is . The product's dosage form is and is administered via form.

Labeler Name: White Manufacturing Inc. Dba Micro-west

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: White Manufacturing Inc. Dba Micro-west
Labeler Code: 61657
Start Marketing Date: 08-30-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Hpz Product Label Images

Hpz Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Echinacea 3XGelsemium 12XHydrastis 3XHypericum 3XLycopodium 12XNat mur 12XNitricum ac 12XRamunc bulb 12XRhus Tox 12XThuja 12X

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Purpose

FOR THE TEMPORARY RELIEF OF COLD SORES,FEVER BLISTERS

Warning

WARNINGS: STOP USE AND CALL A DOCTOR if symptoms persist or worsen. IF PREGNANT OR BREAST FEEDING, consult a healthcare professional before use. CONTAINS ALCOHOL: in case of accidental overdose, consult a poison control center immediately.

Other Safety Information

OTHER INFORMATION: Tamper resistant for your protection. Use only if safety seal is intact.

Directions

DIRECTIONS: Take 6 drops orally, 4 times a day. For ages 2 to adult

Inactive Ingredients

Alcohol 20% v/vPurified water

Indications

INDICATIONS: For the temporary relief of cold sores, fever blisters

Manufacture

MANUFACTURED FOR:MICRO-WESTP. O. BOX 950DOUGLAS, WY 826331307-358-5066

* Please review the disclaimer below.