NDC 49035-107 Blackberry Vanilla Hand Sanitizer Bodycology

NDC Product Code 49035-107

NDC CODE: 49035-107

Proprietary Name: Blackberry Vanilla Hand Sanitizer Bodycology 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.

NDC Code Structure

  • 49035 - Wal-mart Stores Inc
    • 49035-107 - Blackberry Vanilla Hand Sanitizer

NDC 49035-107-02

Package Description: 1 BOTTLE, PLASTIC in 1 PACKAGE > 30 mL in 1 BOTTLE, PLASTIC (49035-107-01)

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

NDC Product Information

Blackberry Vanilla Hand Sanitizer Bodycology with NDC 49035-107 is a product labeled by Wal-mart Stores Inc. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1047755.

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)
  • CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • GELATIN (UNII: 2G86QN327L)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • ULTRAMARINE BLUE (UNII: I39WR998BI)
  • FD&C RED NO. 4 (UNII: X3W0AM1JLX)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Product Labeler Information

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

Labeler Name: Wal-mart Stores Inc
Labeler Code: 49035
Start Marketing Date: 05-21-2013 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.

Blackberry Vanilla Hand Sanitizer Bodycology Product Label Images

Blackberry Vanilla Hand Sanitizer Bodycology 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     PurposeAlcohol 75%          Antiseptic

Otc - Purpose

Uses To decrease bacteria on the skin.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Indications & Usage

Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

Warnings

WarningsFor external use only.FLAMMABLE. Keep away from flame or high heat.When using this productAvoid contact with eyes. If contact occurs, flush eyes with water.Avoid contact with broken skin

Dosage & Administration

DirectionsWet hands thoroughly with product and allow to dry without wiping.For children under 6, use only under adult supervision.Not recommended for infants.

Inactive Ingredient

Inactive ingredients: Water (Aqua, Eau), Fragrance (Parfum), Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Gelatin, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Ultramarines (CI 77007).May Contain: FD&C Red No. 4 (CI 14700), FD&C Yellow No. 5 (CI 19140), FD&C Blue No. 1 (CI 42090), D&C Red No. 33 (CI 17200).

* Please review the disclaimer below.