NDC 72701-105 Bliss Gvs Children


NDC Product Code 72701-105

NDC CODE: 72701-105

Proprietary Name: Bliss Gvs Children 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: Glycerin 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This product is used to relieve occasional constipation. Glycerin belongs to a class of drugs known as hyperosmotic laxatives. It works by drawing water into the intestines. This effect usually results in a bowel movement within 15 to 60 minutes. For adults, the normal frequency of bowel movements varies from once daily to 1 to 2 times weekly. For preschool-aged children, the normal frequency of bowel movements varies from once daily to once every other day. Constipation is best treated by drinking plenty of fluids, eating foods high in fiber, and exercising regularly.

NDC Code Structure

NDC 72701-105-12


NDC 72701-105-25


NDC Product Information

Bliss Gvs Children with NDC 72701-105 is a a human over the counter drug product labeled by Bliss Gvs Pharma Limited. The generic name of Bliss Gvs Children is glycerin. The product's dosage form is suppository and is administered via rectal form.

Labeler Name: Bliss Gvs Pharma Limited

Dosage Form: Suppository - A solid body of various weights and shapes, adapted for introduction into the rectal orifice of the human body; they usually melt, soften, or dissolve at body temperature.

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.

Bliss Gvs Children 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.

  • GLYCERIN 1.2 g/1

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.

  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

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

  • Rectal - Administration to the rectum.

Product Labeler Information

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

Labeler Name: Bliss Gvs Pharma Limited
Labeler Code: 72701
FDA Application Number: part334 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 01-20-2020 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: 12-31-2021 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.

Bliss Gvs Children Product Label Images

Bliss Gvs Children 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


Drug Facts

TAMPER EVIDENT: DO NOT USE IF SEALED WRAPPER AROUND SUPPOSITORIES IS BROKEN OR MISSINGManufactured and Marketed by:BLISS GVS PHARMA LTD.102, Hyde Park, Saki Vihar Road, Andheri (E)Mumbai-400 072, INDIAEmail: info@blissgvs.com • www.blissgvs.com

Otc - Active Ingredient

Active ingredient (in each suppository)Glycerin USP, 1.2 grams

Otc - Purpose


Indications & Usage

  • Usesfor relief of occasional constipationthis product usually produces bowel movement in 1/4 to 1 hour


WarningsFor rectal use only

Otc - Do Not Use

Do not use for longer than one week unless directed by a doctor

Otc - Ask Doctor

  • Ask a doctor before use if the child hasabdominal pain, nausea or vomitinga sudden change in bowel habits lasting more than 2 weeks

Otc - When Using

When using this product your child may have rectal discomfort or a burning sensation

Otc - Stop Use

  • Stop use and ask a doctor if the child hasrectal bleedingno bowel movement after using this productThese may indicate a serious condition.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

  • Directionschildren 2 to under 6 years of age: 1 suppository once dailychildren under 2 years: ask a doctorinsert suppository well up into rectum and retain for 15 minutesit need not melt to produce laxative action

Storage And Handling

Other informationkeep away from excessive heat.

Inactive Ingredient

Inactive ingredients purified water, sodium stearate

Otc - Questions

Questions or Comments? Call


* Please review the disclaimer below.