NDC 82229-001 Reset U

Hovenia Dulcis Thunb.

NDC Product Code 82229-001

NDC 82229-001-01

Package Description: 75 mL in 1 BOTTLE, GLASS

NDC Product Information

Reset U with NDC 82229-001 is a a human over the counter drug product labeled by Doctor Care. The generic name of Reset U is hovenia dulcis thunb.. The product's dosage form is liquid and is administered via topical form.

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.

Reset U 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.

  • SCHISANDRA CHINENSIS WHOLE (UNII: RM13YIU944)
  • ARTEMISIA CAPILLARIS WHOLE (UNII: 852FKP35KV)
  • NASHIPATI (UNII: SHY4TJD066)
  • PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C)
  • CRATAEGUS PINNATIFIDA WHOLE (UNII: TMT0402DF6)
  • CITRUS RETICULATA WHOLE (UNII: O0OX7CMF92)
  • WOLFIPORIA COCOS WHOLE (UNII: Y1I7Z6FF4R)
  • ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)
  • PRUNUS MUME FLOWER (UNII: 2N8872050J)
  • ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)
  • CIRSIUM JAPONICUM (UNII: WCA3C9S0OM)
  • RUBUS COREANUS WHOLE (UNII: 8X91IS0Z3R)
  • ZIZIPHUS JUJUBA VAR. INERMIS WHOLE (UNII: 7E3OM4YS3V)
  • GLYCYRRHIZA URALENSIS WHOLE (UNII: 8XW1DS8UIR)

Administration Route(s)

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

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Doctor Care
Labeler Code: 82229
Marketing Category: UNAPPROVED DRUG OTHER - 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: 09-16-2021 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.

Reset U Product Label Images

Reset U 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

HOVENIA DULCIS THUNB. 19%

Purpose

Hangover

Uses

Helps relieve headache, fatigue, nausea, vomiting caused from consumption of alcohol

When Using This Product,

Do not exceed recommended dosage

Stop Use And Ask A Doctor If

Symptoms last for more than 2 weeks

Keep Out Of Reach Of Children

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

Drink one bottle a day.

Other Information

Store at room temperature

Inactive Ingredients

PUERARIA MONTANA VAR. LOBATA ROOT, CRATAEGUS PINNATIFIDA WHOLE, CIRSIUM JAPONICUM WHOLE, CITRUS RETICULATA WHOLE, WOLFIPORIA COCOS WHOLE, ATRACTYLODES LANCEA ROOT, SCHISANDRA CHINENSIS WHOLE, RUBUS COREANUS WHOLE, ASTRAGALUS PROPINQUUS ROOT, ZIZIPHUS JUJUBA VAR. INERMIS WHOLE, GLYCYRRHIZA URALENSIS WHOLE, ARTEMISIA CAPILLARIS WHOLE, PRUNUS MUME FLOWER, NASHIPATI, FRUCTOOLIGOSACCHARIDE

* Please review the disclaimer below.