NDC 11822-7800 First Aid Burn Relief Rite Aid

NDC Product Code 11822-7800

NDC CODE: 11822-7800

Proprietary Name: First Aid Burn Relief Rite Aid 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

11822 - Rite Aid
- 11822-7800 - First Aid Burn Relief
  - 11822-7800-4
  - 11822-7800-5

NDC 11822-7800-5

Package Description: 170 g in 1 CAN

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

NDC Product Information

First Aid Burn Relief Rite Aid with NDC 11822-7800 is a product labeled by Rite Aid. The generic name of First Aid Burn Relief Rite Aid is . The product's dosage form is and is administered via form.

Labeler Name: Rite Aid

Dosage Form: -

Product Type: 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.

Inactive Ingredient(s)

ALOE VERA LEAF (UNII: ZY81Z83H0X)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
DISODIUM COCOAMPHODIPROPIONATE (UNII: 6K8PRP397M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALCOHOL (UNII: 3K9958V90M)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)

Product Labeler Information

Labeler Name: Rite Aid
Labeler Code: 11822
Start Marketing Date: 11-21-2011 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: 12-31-2019 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 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.

First Aid Burn Relief Rite Aid Product Label Images

image description - label

First Aid Burn Relief Rite Aid 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
Uses
Warnings
When Using This Product
Keep Out Of Reach Of The Children
Directions
Inactive Ingredients

Active Ingredient Purpose

Lidocaine 0.5% External analgesic

Uses

Temporarily relieves pain and itching due to• sunburn • minor burns • minor cuts • scrapes • insect bites • minor skin irritation

Warnings

For external use only

When Using This Product

Keep out of your eyesuse only as directeddo not puncture or incinerate. Contents under pressure. Do not store at temperature above 120F.

Keep Out Of Reach Of The Children

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

Directions

• shake well• adults and children 2 years of age and older: apply to affected area, not more than 3 to 4 times daily• children under 2 years of age: ask a doctor• to apply to face, spray into palm of hand and gently apply

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Carbomer, Diazolidinyl Urea, Disodium Cocoamphodipropionate, Disodium EDTA, Glycerin, Methylparaben, Propylene Glycol, Propylparaben, SD Alcohol 40, Simethicone, Tocopheryl Acetate, Triethanolamine