Sunmark Isopropyl Rubbing Alcohol
Isopropyl Alcohol
Strategic Sourcing Services Llc
Human Otc Drug
NDC 49348-030Sunmark Isopropyl Rubbing Alcohol also known as Isopropyl Alcohol is a human otc drug labeled by 'Strategic Sourcing Services Llc'. National Drug Code (NDC) number for Sunmark Isopropyl Rubbing Alcohol is 49348-030. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Sunmark Isopropyl Rubbing Alcohol drug includes Isopropyl Alcohol - 70 L/100L . The currest status of Sunmark Isopropyl Rubbing Alcohol drug is Active.
Drug Information:
| Drug NDC: | 49348-030 |
| 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: | Sunmark Isopropyl Rubbing Alcohol |
| 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: | Isopropyl Alcohol |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Strategic Sourcing Services 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: | ISOPROPYL ALCOHOL - 70 L/100L
|
| 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: | 28 Jun, 2012 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 03 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: | 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: | Strategic Sourcing Services LLC
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 808520
|
| 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. |
| UPC: | 0010939138330
|
| UPC stands for Universal Product Code. |
| UNII: | ND2M416302
|
| 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 |
|---|
| 49348-030-40 | 3.8 L in 1 BOTTLE (49348-030-40) | 13 Dec, 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 first aid antiseptic
Product Elements:
Sunmark isopropyl rubbing alcohol isopropyl alcohol water isopropyl alcohol isopropyl alcohol
Indications and Usage:
Uses first aid to help prevent infection in minor cuts, scrapes, and burns. for rubbing massage and as an external stimulant.
Warnings:
Warnings for external use only. use in well ventilated area. fumes may be harmful. do not use in the eyes or apply over a large area of the body when used as an antiseptic. in case of deep or puncture wounds, animal bites, or serious burns, consult a doctor. when using this product: do not apply to irritated skin and avoid getting into eyes or mucous membranes. stop use and consult a doctor if the condition persists or gets worse. do not use longer than 1 week unless directed by a doctor. discontinue use if excessive irritation of the skin develops. keep out of reach of children. in case of accidental overdose, seek professional assistance or contact a poison control center immediately. in case of eye contact, flush eyes with running water for 15 minutes.
Do Not Use:
Warnings for external use only. use in well ventilated area. fumes may be harmful. do not use in the eyes or apply over a large area of the body when used as an antiseptic. in case of deep or puncture wounds, animal bites, or serious burns, consult a doctor. when using this product: do not apply to irritated skin and avoid getting into eyes or mucous membranes. stop use and consult a doctor if the condition persists or gets worse. do not use longer than 1 week unless directed by a doctor. discontinue use if excessive irritation of the skin develops. keep out of reach of children. in case of accidental overdose, seek professional assistance or contact a poison control center immediately. in case of eye contact, flush eyes with running water for 15 minutes.
When Using:
When using this product: do not apply to irritated skin and avoid getting into eyes or mucous membranes.
Dosage and Administration:
Directions for antiseptic use: apply a small amount of this product to the affected area 1 to 3 times daily. may be covered with sterile bandage. if bandaged let dry first. for rubbing or massage use: apply compound externally on body until liquid has been absorbed or has been evaporated.
Stop Use:
Stop use and consult a doctor if the condition persists or gets worse. do not use longer than 1 week unless directed by a doctor. discontinue use if excessive irritation of the skin develops.
Package Label Principal Display Panel:
Sunmark isopropyl rubbing alcohol 70% usp first aid antiseptic to help prevent infection in minor cuts, scrapes, and burns for rubbing, massaging and sponge baths. warning: flammable, keep away from spark, heat or flame distributed by mckesson, one post street, san francisco, ca 94104 money back guarantee 128 fl oz (1 gal) 3.8 l
Sunmark isopropyl alcohol 70% usp 128oz (49348-030-40) isopropyl alcohol