NDC 61657-0003 Allerhale

Ars Alb, Phos, Nux Vom, Puls, Sulph, Eup, Sol, Echi, Bapt

NDC Product Information

Allerhale with NDC 61657-0003 is a a human over the counter drug product labeled by White Manufacturing Inc. Dba Micro West. The generic name of Allerhale is ars alb, phos, nux vom, puls, sulph, eup, sol, echi, bapt. The product's dosage form is liquid and is administered via oral form.

Labeler Name: White Manufacturing Inc. Dba Micro West

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Allerhale Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ARSENIC TRIOXIDE 12 [hp_X]/30mL
  • PHOSPHORUS 12 [hp_X]/30mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/30mL
  • ONION 12 [hp_X]/30mL
  • PULSATILLA VULGARIS 12 [hp_X]/30mL
  • SULFUR 12 [hp_X]/30mL
  • EUPHRASIA STRICTA 12 [hp_X]/30mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 12 [hp_X]/30mL
  • ECHINACEA, UNSPECIFIED 3 [hp_X]/30mL
  • GARLIC 3 [hp_X]/30mL
  • BAPTISIA TINCTORIA 3 [hp_X]/30mL

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)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

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
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-01-2011 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: 12-31-2022 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: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Allerhale Product Label Images

Allerhale 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

Allium cepa 12XAllium sat 3XAmbrosia 12XArsenicum alb 12XBaptisia 3XEchinacea 3XEuphresia 12XNux vom 12XPhosphorus 12XPulsatilla 12XSolidago 12XSulphur

Purpose

ITCHING,BURNING, WATERY EYES, SNEEZING

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Indications

INDICATIONS: FOR THE TEMPORARY RELIEF OF ITCHING, BURNING, WATERY EYES, SNEEZING, AND WATERY NOSE

Warning

WARNING:Stop use and call a doctor if symptoms persist or worsen. If pregnant or breast feeding, consult a healthcare professional. Contains alcohol: In case of accidental overdoseconsult a poison control center immediately

Directions

DIRECTIONS:TAKE 6 DROPS ORALLY, 4 TIMES A DAY. FOR AGES 2 TO ADULT

Inactive Ingredient

ALCOHOL (20%V/V),PURIFIED WATER

Manufacture

MANUFACTURED FOR MICRO WESTDOUGLAS, WY 826331-307-358-5066

* Please review the disclaimer below.