NDC 30805-008 Symmetry Foaming Hand Sanitizer-unscented

NDC Product Code 30805-008

NDC 30805-008-04

Package Description: 1200 mL in 1 BAG

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Symmetry Foaming Hand Sanitizer-unscented with NDC 30805-008 is a product labeled by Buckeye International, Inc.. The generic name of Symmetry Foaming Hand Sanitizer-unscented is . The product's dosage form is and is administered via form.

Labeler Name: Buckeye International, Inc.

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)
  • ALOE (UNII: V5VD430YW9)

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
Start Marketing Date: 07-12-2010 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".

* Please review the disclaimer below.

Symmetry Foaming Hand Sanitizer-unscented Product Label Images

Symmetry Foaming Hand Sanitizer-unscented 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 ingredient                                                PurposeEthyl Alcohol 62%.............................................Antimicrobial

Indications & Usage

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


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

Storage And Handling

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.