NDC 30805-009 Symmetry Foaming Hand Sanitizer-fragrance Free With Aloe And Vitamin E

Alcohol

NDC Product Code 30805-009

NDC CODE: 30805-009

Proprietary Name: Symmetry Foaming Hand Sanitizer-fragrance Free With Aloe And Vitamin E 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: Alcohol 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

NDC 30805-009-04

Package Description: 1200 mL in 1 BAG

NDC 30805-009-05

Package Description: 50 mL in 1 BOTTLE, PUMP

NDC 30805-009-07

Package Description: 550 mL in 1 BOTTLE, PUMP

NDC 30805-009-08

Package Description: 700 mL in 1 BAG

NDC 30805-009-09

Package Description: 1000 mL in 1 BAG

NDC 30805-009-10

Package Description: 750 mL in 1 BAG

NDC 30805-009-11

Package Description: 3785 mL in 1 BOTTLE

NDC Product Information

Symmetry Foaming Hand Sanitizer-fragrance Free With Aloe And Vitamin E with NDC 30805-009 is a a human over the counter drug product labeled by Buckeye International, Inc.. The generic name of Symmetry Foaming Hand Sanitizer-fragrance Free With Aloe And Vitamin E is alcohol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Buckeye International, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Symmetry Foaming Hand Sanitizer-fragrance Free With Aloe And Vitamin E Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ALCOHOL 62 mL/100mL

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • ALOE (UNII: V5VD430YW9)
  • ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
  • PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
  • PEG-8 DIMETHICONE (UNII: GIA7T764OD)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Buckeye International, Inc.
Labeler Code: 30805
FDA Application Number: part333A What is the FDA Application Number?
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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 10-04-2011 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: 12-31-2022 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: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Symmetry Foaming Hand Sanitizer-fragrance Free With Aloe And Vitamin E Product Label Images

Symmetry Foaming Hand Sanitizer-fragrance Free With Aloe And Vitamin E 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

Otc - Active Ingredient

Active IngredientEthyl Alcohol 62%

Otc - Purpose

PurposeAntimicrobial

Indications & Usage

UsesHand sanitizer to help reduce bacteria on the skin that could cause diseaseRecommended for repeated use

Warnings

WarningsFlammable. Keep away from fire or flame.For external use only.

Otc - When Using

When using this product do not use in or near eyes.If in eyes, flush thoroughly with water.

Adverse Reactions

If irritation or rash appears and persists, stop use and see a physician.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, call a physician or Poison Control Center immediately.

Dosage & Administration

DirectionsDispense an adequate amount of hand sanitizerRub hands together until completely dry

Safe Handling Warning

Other informationDo not store above 110 F (43 C)May discolor some fabrics or surfaces

Inactive Ingredient

Inactive ingredientsWater (Aqua), PEG-10 Dimethicone, PEG-12 Dimethicone, PEG-8 Dimethicone, Glycerin, Propylene Glycol, Isopropyl Myristate, Aloe, and Tocopheryl Acetate.

Otc - Questions

Questions?Call: Buckeye International, Inc. 314-291-1900Monday through Friday 8:00 a.m. to 5:00 p.m. CST

* Please review the disclaimer below.