NDC 69842-762 Cvs Non-drowsy Flu Relief

Anas Barbariae Hepatis Et Cordis Extractum

NDC Product Code 69842-762

NDC CODE: 69842-762

Proprietary Name: Cvs Non-drowsy Flu Relief What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Anas Barbariae Hepatis Et Cordis Extractum What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Product Characteristics

WHITE (C48325)
Shape: ROUND (C48348)
10 MM

NDC Code Structure

  • 69842 - Cvs Pharmacy

NDC 69842-762-14

Package Description: 1 BLISTER PACK in 1 CARTON > 30 PILL in 1 BLISTER PACK

NDC Product Information

Cvs Non-drowsy Flu Relief with NDC 69842-762 is a a human over the counter drug product labeled by Cvs Pharmacy. The generic name of Cvs Non-drowsy Flu Relief is anas barbariae hepatis et cordis extractum. The product's dosage form is pill and is administered via oral form.

Dosage Form: Pill - A small, round solid dosage form containing a medicinal agent intended for oral administration.

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.

Cvs Non-drowsy Flu Relief 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.

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.

  • COPOVIDONE K25-31 (UNII: D9C330MD8B)
  • SORBITOL (UNII: 506T60A25R)

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: Cvs Pharmacy
Labeler Code: 69842
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: 06-15-2021 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 - NO 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.

Cvs Non-drowsy Flu Relief Product Label Images

Cvs Non-drowsy Flu Relief 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 Ingredient

Active Ingredient*PurposeAnas barbariae 200CK HPUSReduce the duration and severity of flu like symptomsThe letters “HPUS” indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States.


Reduce the duration and severity of flu like symptoms*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.


According to homeopathic indications, this ingredient provides temporary relief of flu symptoms such as: • body aches, headache, fever, chills and fatigue, after serious causes have been ruled out by a physician.* These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.


WarningsA PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES. • This product is intended to complement, not replace, standard medical treatment.• Initial worsening of symptoms may occur.

Pregnant Or Breast-Feeding

• If pregnant or breast-feeding, ask a health professional before use.

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.

Stop Use And Ask A Doctor If:

Stop use and ask a doctor if:• You experience worsening symptoms. • Any new symptoms appear. • Symptoms last longer than 3 days.


Directions• Suitable for adults and children ages 12 and over. Children under the age of 12: Consult a physician before use. Dissolve entire tablet under tongue OR chew tablet and swallow. • Do not swallow tablet whole. • Take 1 tablet every six hours. • Take at least 10 minutes before or at least 10 minutes after eating or drinking. • Homeopathic remedies may not be effective for everyone. Individual results may vary.

Other Information

Other information• Do not use if blister seal is broken. • Store at room temperature 15o to 30o C (59o to 86o F). • Active ingredients are micro-diluted in accordance with the Homeopathic Pharmacopoeia of the United States and are therefore non-toxic with no known side effects or contraindications.

Inactive Ingredients

Inactive ingredientsCopovidone, Crospovidone, Lactose, Magnesium stearate, Mannitol, Microcrystalline cellulose, Silicon dioxide, Sorbitol.

* Please review the disclaimer below.