NDC 50730-1033 Isopropyl Alcohol Prep Pad
NDC Product Code 50730-1033
Proprietary Name: Isopropyl Alcohol Prep Pad What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 50730 - H And P Industries, Inc. Dba Triad Group
- 50730-1033 - Isopropyl Alcohol Prep Pad
NDC 50730-1033-1
Package Description: 140 PACKET in 1 BOX > 1 SWAB in 1 PACKET
NDC Product Information
Isopropyl Alcohol Prep Pad with NDC 50730-1033 is a product labeled by H And P Industries, Inc. Dba Triad Group. The generic name of Isopropyl Alcohol Prep Pad is . The product's dosage form is and is administered via form.
Labeler Name: H And P Industries, Inc. Dba Triad Group
Inactive Ingredient(s)
About the Inactive Ingredient(s)The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
- WATER (UNII: 059QF0KO0R)
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: H And P Industries, Inc. Dba Triad Group
Labeler Code: 50730
Start Marketing Date: 09-28-2007 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: I - INACTIVATED, the listing data was inactivated by the FDA. What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
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Isopropyl Alcohol Prep Pad Product Label Images
Isopropyl Alcohol Prep Pad Product Labeling Information
The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
Product Labeling Index
- Active Ingredient
- Purpose
- Use
- Warnings
- Do Not Use
- Stop Use
- Keep Out Of Reach Of Children
- Directions
- Other Information
- Inactive Ingredient
- Package Information
Active Ingredient
Isopropyl Alcohol 70% v/v
Purpose
Antiseptic
Use
For preparation of the skin prior to an injection
Warnings
For external use only. Flammable, keep away from fire or flame.
Do Not Use
- With electrocautery proceduresin the eyes
Stop Use
If irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wipe injection site vigorously and discard
Other Information
Store at room temperature 15° - 30° C (59° - 86° F)
Inactive Ingredient
Purified water
Package Information
NDC 50730-1033-1Kroeger®
Quality GuaranteedALCOHOL SWABSSoft Antiseptic Swabs saturated with Isopropyl Alcohol, 70% v/vANTISEPTIC FOR PREPARATION OF THE SKIN PRIOR TO INJECTIONIndividually wrapped140 SWABSQuality GuaranteedIf you are not completely satisfied with this product, return it for a refund or replacement.Comments or Questions?800-632-6900www.kroeger.comDISTRIBUTED BY THE KROEGER CO.,CINCINNATI, OHIO 45202Questions? Please Call: 1-800-491-7448
* Please review the disclaimer below.
