Silver Nitrate Applicators
Arzol Chemical Company
Human Prescription Drug
NDC 12870-0001Silver Nitrate Applicators is a human prescription drug labeled by 'Arzol Chemical Company'. National Drug Code (NDC) number for Silver Nitrate Applicators is 12870-0001. This drug is available in dosage form of Stick. The names of the active, medicinal ingredients in Silver Nitrate Applicators drug includes Potassium Nitrate - 25 mg/100mg Silver Nitrate - 75 mg/100mg . The currest status of Silver Nitrate Applicators drug is Active.
Drug Information:
| Drug NDC: | 12870-0001 |
| 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: | Silver Nitrate Applicators |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Prescription 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: | Silver Nitrate Applicators |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Arzol Chemical Company |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Stick |
| 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: | POTASSIUM NITRATE - 25 mg/100mg
SILVER NITRATE - 75 mg/100mg
|
| 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: | 01 Jan, 1937 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 14 Jan, 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, 2024 |
| 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: | Arzol Chemical Company
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1117536
|
| 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: | RU45X2JN0Z
95IT3W8JZE
|
| 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 |
|---|
| 12870-0001-1 | 10 PACKET in 1 BOX (12870-0001-1) / 10 APPLICATOR in 1 PACKET / 100 mg in 1 APPLICATOR | 01 Jan, 1937 | N/A | No |
| 12870-0001-2 | 100 APPLICATOR in 1 VIAL (12870-0001-2) / 100 mg in 1 APPLICATOR | 01 Jan, 1937 | 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. |
Product Elements:
Silver nitrate applicators silver nitrate applicators potassium nitrate nitrate ion silver nitrate silver cation
Indications and Usage:
Indications on the skin, applications of silver nitrate are recommended for cauterization of wounds and sluggish ulcers, also for removal of granulation tissue and warts. on mucous membranes, silver nitrate may be applied to small ulcers and aphthae in the mouth resulting from injury or stomatitis, to infected tonsils, to rectal fissures and fistulae, and to vaginal or cervical ulcerations or erosions. epistaxis may be controlled by direct application to the site of hemorrhage within the nostrils.
Warnings:
Side effects silver nitrate blackens the tissues to which it is applied but this discoloration gradually disappears. in the case of applicators, poisoning from ingestion is rare.
Poison
Caution: federal law prohibits dispensing without prescription. do not open this box or dispense packets or applicators separately.
Poison
Caution: federal law prohibits dispensing without prescription. do not dispense packets or applicators separately.
Not for resale
Caution: federal law prohibits dispensing without prescription. do not open this tube or dispense applicators separately.
Poison
Warnings and Cautions:
Warning: keep out of reach of children. keep in dry and dark place. do not use on the eyes.
Warning: do not use on the eyes. keep out of reach of children. keep in a dry and dark place.
Warning: do not use on the eyes. keep out of reach of children. keep in a dry and dark place.
General Precautions:
Special properties the combination of silver nitrate with potassium nitrate has been called toughened silver nitrate , also lunar caustic . when the tip of the applicator is impregnated with this compound, as in arzol , the silver nitrate can be applied quickly and conveniently to the precise area to be treated without spread of the escharotic to adjacent healthy tissues. exposure to light causes the silver in the tip to oxidize and turn brown in color. this discoloration does not affect the therapeutic action of the tip and the oxidized film readily dissolves when dipped in water. moisture has a deteriorating effect on the tip. it may cause it to break or loosen from the applicator; therefore the applicators should be kept in a dry place. caution: silver nitrate is a caustic compound, the improper use of which may cause chemical burns. silver nitrate mixes with body fluids; this mixture is caustic and tissue damage may result if not removed quickly. contact of silver nitrate applicato
Read more...rs on neonates (as in use on the umbilicus) and on thin delicate skin should be extremely short in duration.
Dosage and Administration:
Application arzol may be applied direct to mucous membranes and other moist surfaces. in the case of dry skin, the applicator tip should be dipped in water immediately before use. apply carefully to the area to be treated. do not use on the eyes.
Dosage Forms and Strength:
Silver nitrate 75% potassium nitrate 25%
Silver nitrate 75% potassium nitrate 25%
(silver nitrate 75%) (potassium nitrate 25%)
Silver nitrate 75% potassium nitrate 25%
Adverse Reactions:
Hazards long continued applications to large areas may produce argyria, a slate-blue discoloration of the skin and mucous membranes.
Description:
For simplified silver nitrate therapy arzol silver nitrate applicators provide a simple and convenient means of treating small lesions of the skin and mucous membranes. on contact with living tissue, silver nitrate acts as an escharotic. deep action is avoided by the formation of a dense surface film of coagulated albumin. silver nitrate is a powerful chemical germicide. despite precipitation, it retains substantial germicidal potency even in the presence of large quantities of albuminous material, possibly by gradually redissolving the silver.
For simplified silver nitrate therapy
For simplified silver nitrate therapy
For simplified silver nitrate therapy
How Supplied:
Availability arzol silver nitrate applicators are supplied in boxes of 100 containing 10 packets each with 10 applicators; also, in plastic tubes containing 100 applicators.
100 applicators
Ten (10) applicators
Package Label Principal Display Panel:
Arzol box packaging arzol® silver nitrate applicators silver nitrate 75% potassium nitrate 25% for simplified silver nitrate therapy poison caution: federal law prohibits dispensing without prescription. do not open this box or dispense packets or applicators separately. warning: keep out of reach of children. keep in dry and dark place. do not use on the eyes. 100 applicators antidote in case of accidental poisoning, follow these directions. external - eye exposure: first: wash out the eye with lukewarm water for at least fifteen (15) minutes then: call your physician or go to your nearest emergency room. skin exposure: first: wash the areas very thoroughly with soap and water then: call your physician. internal: first: give one (1) glass of milk or water then: call your physician or go to your nearest emergency room. stability precautions light causes the silver in the tip to oxidize and turn brown in color. this does not affect the therapeutic action of the tip and the oxidized film readily dissolves when dipped in water. moisture has a deteriorating effect on the tip. it will cause the tip to break or loosen from the applicator; therefore the applicators should be kept in a dry and dark place.
Arzol inner envelope packaging arzol® silver nitrate applicators (silver nitrate 75%) (potassium nitrate 25%) for simplified silver nitrate therapy poison ten (10) applicators caution: federal law prohibits dispensing without prescription. do not dispense packets or applicators separately. warning: do not use on the eyes. keep out of reach of children. keep in a dry and dark place. not for resale antidote in case of accidental poisoning, follow these directions: external: eye exposure: first: wash out the eye with lukewarm water for at least fifteen (15) minutes then call your physician or go to your nearest emergency room. skin exposure: first: wash the area very thoroughly with soap and water then call your physician. internal: first: give one (1) glass of milk or water then call your physician or go to your nearest emergency room. stability precautions light causes the silver in the tip to oxidize and turn brown in color. this does not affect the therapeutic action of the tip and the oxidized film readily dissolves when dipped in water. moisture has a deteriorating effect on the tip. it will cause the tip to break or loosen from the applicator; therefore the applicators should be kept in a dry and dark place.
Arzol vial packaging arzol silver nitrate applicators silver nitrate 75% potassium nitrate 25% for simplified silver nitrate therapy caution: federal law prohibits dispensing without prescription. do not open this tube or dispense applicators separately. warning: do not use on the eyes. keep out of reach of children. keep in a dry and dark place. poison in case of accidental poisoning, follow these directions: antidote external: eye exposure: first: wash out the eye with lukewarm water for at least fifteen (15) minutes then call your physician or go to your nearest emergency room. skin exposure: first: wash the area very thoroughly with soap and water then call your physician. internal: first: give one (1) glass of milk or water then call your physician or go to your nearest emergency room.