Citrus Sunshine
Alcohol
Personal Care Products Llc
Human Otc Drug
NDC 29500-9355Citrus Sunshine also known as Alcohol is a human otc drug labeled by 'Personal Care Products Llc'. National Drug Code (NDC) number for Citrus Sunshine is 29500-9355. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Citrus Sunshine drug includes Alcohol - 26.36 g/44mL . The currest status of Citrus Sunshine drug is Active.
Drug Information:
| Drug NDC: | 29500-9355 |
| 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: | Citrus Sunshine |
| 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: | Alcohol |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Personal Care Products Llc |
| 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: | ALCOHOL - 26.36 g/44mL
|
| 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 NOT 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: | 23 Mar, 2017 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 22 Dec, 2025 |
| 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: | part333A |
| 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: | Personal Care Products LLC
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 247835
|
| 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: | 3K9958V90M
|
| 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 |
|---|
| 29500-9355-1 | 44 mL in 1 BOTTLE, PLASTIC (29500-9355-1) | 23 Mar, 2017 | 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 antimicrobial
Product Elements:
Laughing linen alcohol alcohol alcohol water aloe vera leaf carboxypolymethylene glycerin propylene glycol trolamine .alpha.-tocopherol acetate fd&c blue no. 1 citrus sunshine alcohol alcohol alcohol water aloe vera leaf carboxypolymethylene glycerin propylene glycol trolamine .alpha.-tocopherol acetate fd&c yellow no. 5 love you berry much alcohol alcohol alcohol water aloe vera leaf carboxypolymethylene glycerin propylene glycol trolamine .alpha.-tocopherol acetate fd&c red no. 40 d&c red no. 33 coconut lime alcohol alcohol alcohol water aloe vera leaf carboxypolymethylene glycerin propylene glycol trolamine .alpha.-tocopherol acetate fd&c yellow no. 5 fd&c blue no. 1 frisky cinnamon alcohol alcohol alcohol water aloe vera leaf carboxypolymethylene glycerin propylene glycol trolamine .alpha.-tocopherol acetate fd&c red no. 40 foxy citrus alcohol alcohol alcohol water aloe vera leaf carboxypolymethylene glycerin propylene glycol trolamine .alpha.-tocopherol acetate fd&c yellow no. 5 fresh breeze alcohol alcohol alcohol water aloe vera leaf carboxypolymethylene glycerin propylene glycol trolamine .alpha.-tocopherol acetate fd&c blue no. 1 pretty punch alcohol alcohol alcohol water aloe vera leaf carboxypolymethylene glycerin propylene glycol trolamine .alpha.-tocopherol acetate fd&c red no. 40
Indications and Usage:
Use hand sanitizer to help reduce bacteria on skin.
Warnings:
Flammable keep away from heat and flame
When Using:
When using this product avoid contact with eyes. i contact occurs, rinse thoroughly with water.
Dosage and Administration:
Directions wet hands thoroughly with product and rub into skin until dry. children under 6 years of age should be supervised by an adult when using.
Stop Use:
Stop use and ask a doctor if irritation or redness develops.
Package Label Principal Display Panel:
Laughing linen - 9354 citrus sunshine - 9355 love you berry much - 9356 coconut lime - 9357 frisky cinnamon - 9359 foxy citrus - 9360 fresh breeze - 9361 pretty punch - 9362 product labels peel up to see additional drug facts distributed by: personal care products, llc troy, michigan 48084 made in china laughing linen - 9354 citrus sunshine - 9355 love you berry much - 9356 coconut lime - 9357 frisky cinnamon - 9359 foxy citrus - 9360 fresh breeze - 9361 pretty punch - 9362 pc laughing linen 9354 pc citrus sunshine 9355 pc love you berry much 9356 pc coconut lime 9357 pc frisky cinnamon 9359 pc foxy citrus 9360 pc fresh breeze 9361 pc pretty punch 9362