Soothe
Bismuth Subsalicylate
Walgreens
Human Otc Drug
NDC 0363-0073Soothe also known as Bismuth Subsalicylate is a human otc drug labeled by 'Walgreens'. National Drug Code (NDC) number for Soothe is 0363-0073. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Soothe drug includes Bismuth Subsalicylate - 525 mg/30mL . The currest status of Soothe drug is Active.
Drug Information:
| Drug NDC: | 0363-0073 |
| 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: | Soothe |
| 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: | Bismuth Subsalicylate |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Walgreens |
| 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: | BISMUTH SUBSALICYLATE - 525 mg/30mL
|
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | ORAL
|
| 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: | 31 Jan, 2015 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 15 Jan, 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: | part335 |
| 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: | Walgreens
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 308762
|
| 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: | 0311917083872
|
| UPC stands for Universal Product Code. |
| NUI: | M0002611
N0000180183
|
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). |
| UNII: | 62TEY51RR1
|
| 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. |
| Pharmacologic Class EPC: | Bismuth [EPC]
|
| Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`. |
| Pharmacologic Class CS: | Bismuth [CS]
|
| Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient]. |
| Pharmacologic Class: | Bismuth [CS]
Bismuth [EPC]
|
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 0363-0073-08 | 237 mL in 1 BOTTLE, PLASTIC (0363-0073-08) | 31 Jan, 2015 | N/A | No |
| 0363-0073-16 | 473 mL in 1 BOTTLE, PLASTIC (0363-0073-16) | 31 Jan, 2015 | 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 upset stomach reliever/antidiarrheal
Product Elements:
Soothe bismuth subsalicylate bismuth subsalicylate bismuth cation salicylic acid benzoic acid d&c red no. 22 d&c red no. 28 magnesium aluminum silicate water saccharin sodium salicylic acid sodium salicylate sorbic acid methylcellulose (1500 cps)
Indications and Usage:
Uses relieves travelers' diarrhea diarrhea upset stomach due to overindulgence in food and drink, including: heartburn indigestion nausea gas fullness belching
Warnings:
Warnings reye's syndrome : children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. when using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of reye's syndrome, a rare but serious illness. allergy alert: contains salicylate. do not take if you are allergic to salicylates (including aspirin) taking other salicylate products do not use if you have an ulcer a bleeding problem bloody or black stool ask a doctor before use if you have fever mucus in the stool ask a doctor or pharmacist before use if you are taking any drug for diabetes gout arthritis anticoagulation (thinning the blood) when using this product a temporary, but harmless, darkening of the stool and/or tongue may occur. stop use and ask a doctor if symptoms get worse or last more than 2 days ringing in the ears or loss of hearing occurs diarrhea lasts more than 2 days if pregnant or
Read more...breast-feeding, ask a health professional before use. keep out of reach of childen. in case of overdose, get medical help or contact a posion control center right away. (1-800-222-1222)
Do Not Use:
Warnings reye's syndrome : children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. when using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of reye's syndrome, a rare but serious illness. allergy alert: contains salicylate. do not take if you are allergic to salicylates (including aspirin) taking other salicylate products do not use if you have an ulcer a bleeding problem bloody or black stool ask a doctor before use if you have fever mucus in the stool ask a doctor or pharmacist before use if you are taking any drug for diabetes gout arthritis anticoagulation (thinning the blood) when using this product a temporary, but harmless, darkening of the stool and/or tongue may occur. stop use and ask a doctor if symptoms get worse or last more than 2 days ringing in the ears or loss of hearing occurs diarrhea lasts more than 2 days if pregnant or breast-feeding, ask a health professional before use. keep out of reach of childen. in case of overdose, get medical help or contact a posion control center right away. (1-800-222-1222)
When Using:
When using this product a temporary, but harmless, darkening of the stool and/or tongue may occur.
Dosage and Administration:
Directions ml = milliliter shake well before using measure only with dosing cup provided. do not use any other dosing device. keep dosing cup with product adults and children 12 years and over: 30 ml (1 dose) every 1/2 to 1 hour as needed do not exceed 8 doses (240 ml) in 24 hours use until diarrhea stops but not more than 2 days children under 12 years of age: ask a doctor drink plenty of clear fluids to help prevent dehydration caused by diarrhea
Stop Use:
Stop use and ask a doctor if symptoms get worse or last more than 2 days ringing in the ears or loss of hearing occurs diarrhea lasts more than 2 days
Package Label Principal Display Panel:
Principal display panel compare to pepto-bismol® active ingredient soothe® bismuth subsalicylate 525mg / upset stomach reliever / antidiarrheal sugar free alcohol free provides protective coating action to relieves heartburn, indigestion, nausea, upset stomach & diarrhea fl oz (ml) ??this product is not manufactured or distributed by procter & gamble company, pepto-bismol® is a registered trademark of the protecter & gamble company. tamper evident; do not use if printed safety seal around dosage cup or under cap is broken or missing. distributed by: walgreen co. 200 wilmot rd, deerfield, il 60015 walgreens.com
Package label walgreens soothe bismuth subsalicylate 525 mg
Further Questions:
Questions or comments? call 1-877-753-3935 monday-friday 9am-5pm est