Cvs Health Medicated
Witch Hazel
Cvs Pharmacy
Human Otc Drug
NDC 59779-747Cvs Health Medicated also known as Witch Hazel is a human otc drug labeled by 'Cvs Pharmacy'. National Drug Code (NDC) number for Cvs Health Medicated is 59779-747. This drug is available in dosage form of Cloth. The names of the active, medicinal ingredients in Cvs Health Medicated drug includes Witch Hazel - 500 mg/1 . The currest status of Cvs Health Medicated drug is Active.
Drug Information:
| Drug NDC: | 59779-747 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Cvs Health Medicated |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Proprietary Name Base: | Cvs Health |
| The base of the Brand/Proprietary name excluding its suffix. |
| Proprietary Name Suffix: | Medicated |
| A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Witch Hazel |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Cvs Pharmacy |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Cloth |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | WITCH HAZEL - 500 mg/1
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | TOPICAL
|
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | OTC MONOGRAPH FINAL |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. |
| Marketing Start Date: | 24 Nov, 2015 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 06 May, 2026 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Application Number: | part346 |
| 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. |
| Listing Expiration Date: | 31 Dec, 2023 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | CVS Pharmacy
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 844379
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | 101I4J0U34
|
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 59779-747-01 | 1 JAR in 1 CARTON (59779-747-01) / 50 CLOTH in 1 JAR | 24 Nov, 2015 | N/A | No |
| 59779-747-02 | 1 JAR in 1 CARTON (59779-747-02) / 100 CLOTH in 1 JAR | 24 Nov, 2015 | N/A | No |
| 59779-747-10 | 1 PACKAGE in 1 CARTON (59779-747-10) / 10 CLOTH in 1 PACKAGE | 30 Jun, 2022 | N/A | No |
| 59779-747-48 | 1 CARTON in 1 CARTON (59779-747-48) / 48 CLOTH in 1 CARTON | 07 Jul, 2021 | N/A | No |
| 59779-747-96 | 1 PACKAGE in 1 CARTON (59779-747-96) / 96 CLOTH in 1 PACKAGE | 30 Jun, 2022 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Purpose astringent
Product Elements:
Cvs health medicated witch hazel water alcohol glycerin phenoxyethanol aloe decyl glucoside potassium sorbate propylene glycol sodium benzoate citric acid monohydrate witch hazel witch hazel
Indications and Usage:
Uses helps relieve the local itching and discomfort associated with hemorrhoids temporary relief of irritation and burning. aids in protecting irritated anorectal areas.
Warnings:
Warnings for external use only. when using this product do not exceed the recommended daily dosage unless directed by a doctor do not put this product into the rectum by using fingers or any mechanical device or applicator. stop use and ask a doctor if bleeding occurs condition worsens or does not improve within 7 days keep out of reach of children. if swallowed, get medical help or contact poison control center right away. (1-800-222-1222). if pregnant or breast-feeding, ask a health professional before use.
When Using:
When using this product do not exceed the recommended daily dosage unless directed by a doctor do not put this product into the rectum by using fingers or any mechanical device or applicator.
Dosage and Administration:
Directions adult: cleanse the area by gently wiping, patting or blotting. if necessary, repeat until all matter is removed from the area. use up to 6 times daily or after each bowel movement and before applying hemorrhoidal treatments, and then discard children under 12 years of age: consult a doctor do not flush in toilets, dispose of pad in trash after use.
Stop Use:
Stop use and ask a doctor if bleeding occurs condition worsens or does not improve within 7 days
Package Label Principal Display Panel:
Principal display panel cvs health compare to the active ingredient in tucks®* ndc 59779-747-01 medicated pads hemorrhoidal pads with witch hazel hemorrhoidal relief cooling, soothing ph balanced for hemorrhoidal and vaginal care 50 pads *this product is not manufactured or distributed by mcneil-ppc, inc, owner of the registered trademark tucks® cvs health compare to the active ingredient in tucks®* ndc 59779-747-02 medicated pads hemorrhoidal pads with witch hazel hemorrhoidal relief cooling, soothing ph balanced for hemorrhoidal and vaginal care 100 pads value size 100 pads *this product is not manufactured or distributed by mcneil-ppc, inc, owner of the registered trademark tucks® cvs health maximum strength formula medicated wipes to go hemorrhoidal wipes with witch hazel mild, everyday wipes to ease & lessen irritation cooling; soothing; gentle; soft individually wrapped for convenience easy to use for hemorrhoidal & vaginal care 10 medicated wipes cvshealth maximum strength formula medicated wipes hemorrhoidal wipes with witch hazel mild, everyday wipes to ease & lessen irritation cooling: soothing: gentle: soft convenient: easy to use for hemorrhoidal & vaginal care 48 medicated wipes cvs health maximum strength formula medicated wipes hemorrhoidal wipes with witch hazel mild, everyday wipes to ease & lessen irritation cooling; soothing; gentle; soft individually wrapped for convenience easy to use for hemorrhoidal & vaginal care 2 x 48 medicated wipes | 96 total maximum strength formula medicated wipe to go hemorrhoidal wipe with witch hazel 1 medicated wipe label label 1 10ct 48ct 48 ct_2 96ct 1ct