Medimom Lava Yellow Baby Wipes
Noni Extract, Houttuynia Cordata Extract
Medimom Inc.
Human Otc Drug
NDC 82380-102Medimom Lava Yellow Baby Wipes also known as Noni Extract, Houttuynia Cordata Extract is a human otc drug labeled by 'Medimom Inc.'. National Drug Code (NDC) number for Medimom Lava Yellow Baby Wipes is 82380-102. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Medimom Lava Yellow Baby Wipes drug includes Houttuynia Cordata Flowering Top - .1 g/100g Morinda Citrifolia Leaf - .1 g/100g . The currest status of Medimom Lava Yellow Baby Wipes drug is Active.
Drug Information:
| Drug NDC: | 82380-102 |
| 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: | Medimom Lava Yellow Baby Wipes |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| 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: | Noni Extract, Houttuynia Cordata Extract |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Medimom Inc. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Liquid |
| 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: | HOUTTUYNIA CORDATA FLOWERING TOP - .1 g/100g
MORINDA CITRIFOLIA LEAF - .1 g/100g
|
| 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: | UNAPPROVED DRUG OTHER |
| 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: | 06 Jan, 2022 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 07 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. |
| 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: | Medimom Inc.
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | RH041UUZ22
7UOL7P5FF5
|
| 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 |
|---|
| 82380-102-01 | 445 g in 1 POUCH (82380-102-01) | 06 Jan, 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 antiseptic
Product Elements:
Medimom lava yellow baby wipes noni extract, houttuynia cordata extract houttuynia cordata flowering top houttuynia cordata flowering top cupressus sempervirens leaf oil sapindus mukorossi fruit water morinda citrifolia leaf morinda citrifolia leaf hyaluronic acid
Indications and Usage:
Directions â open the cover and use the desired amount of wipes. â use wipes as soon as possible after opening. â wipe the surface area gently. â replace sticker after use to prevent the wipes from drying out
Warnings:
Warnings â flammable. keep away from heat or flame.
Do Not Use:
Warnings â flammable. keep away from heat or flame.
When Using:
When using â when using the product, avoid contact with eyes. in case of contact, rinse eyes thoroughly with water. â» use only as intended and according to the directions of use.
Dosage and Administration:
Uses â hand sanitizer wipes to help reduce bacteria. â for use when soap and water are not available.
Stop Use:
Stop use and ask a doctor â stop use and ask a doctor if you notice the following symptoms: 1)signs of irritation or rash 2)signs of irritation or rash after exposure to sunlight
Package Label Principal Display Panel:
Label 82380 -102-01 82380 -102