NDC 56062-711 Publix Burn Relief Aloe Vera

NDC Product Code 56062-711

NDC 56062-711-19

Package Description: 226 g in 1 BOTTLE, PLASTIC

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

NDC Product Information

Publix Burn Relief Aloe Vera with NDC 56062-711 is a product labeled by Publix Super Markets Inc. The generic name of Publix Burn Relief Aloe Vera is . The product's dosage form is and is administered via form.

Labeler Name: Publix Super Markets 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)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • POLYSORBATE 80 (UNII: 6OZP39ZG8H)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • MENTHOL (UNII: L7T10EIP3A)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Product Labeler Information

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

Labeler Name: Publix Super Markets Inc
Labeler Code: 56062
Start Marketing Date: 07-12-2013 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: 12-31-2019 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.

Publix Burn Relief Aloe Vera Product Label Images

Publix Burn Relief Aloe Vera 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

Lidocaine HCl   0.5%

Purpose

Topical Analgesic

Uses

  • Temporary relief of pain and itchinghelps relieve and soothes pain from sunburn, minor burns, cuts, scrapes, skin irritations and insect bites

Warnings

For external use only

Do Not Use

In large quantities, particularly over raw surfaces or blistered areas.

When Using This Product

  • Avoid contact with eyes

Stop Use And Ask A Doctor If

  • Condition worsens or if symptoms persist for more than 7 days.symptoms clear up and occur again within a few days.

Keep Out Of Reach Of Children

If swallowed get medical help or contact a Poison Control Center right away

Directions

  • Adults and children 2 years of age and older: apply to affected areas not more than 3 to 4 times dailychildren under 2 years of age: do not use, ask a doctor

Inactive Ingredients

Water, Propylene Glycol, Glycerin, Isopropyl Alcohol, Triethanolamine, Polysorbate 80, Carbomer, Aloe Barbadensis Leaf Juice Powder, Menthol, Disodium EDTA, Diazolidinyl Urea, Yellow 5, Blue 1.

* Please review the disclaimer below.