NDC 70708-072 Hand Sanitizer Lol

Hand Sanitizer

NDC Product Code 70708-072

NDC CODE: 70708-072

Proprietary Name: Hand Sanitizer Lol 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: Hand Sanitizer 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.

Product Characteristics


NDC Code Structure

  • 70708 - Gurunanda, Llc

NDC 70708-072-01

Package Description: 60 mL in 1 BOTTLE, SPRAY

NDC Product Information

Hand Sanitizer Lol with NDC 70708-072 is a a human over the counter drug product labeled by Gurunanda, Llc. The generic name of Hand Sanitizer Lol is hand sanitizer. The product's dosage form is spray and is administered via topical form.

Labeler Name: Gurunanda, Llc

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

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.

Hand Sanitizer Lol 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.


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)

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: Gurunanda, Llc
Labeler Code: 70708
Marketing Category: UNAPPROVED DRUG OTHER - 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: 04-01-2021 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 - NO 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.

Hand Sanitizer Lol 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

Isopropyl Alcohol 70 %

Otc - Purpose




Otc - When Using

When using this product do not use in or near the eyes, mouth, or open skin wounds. In case of contact, rinse the area thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or rash appears and lasts for more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (800-222-1222) right away.

Dosage & Administration

-Place enough product on hands to cover all surfaces. Rub hands together until dry.-Shake well before use-Supervise children under 6 years when using this product to avoid swallowing.

Other Safety Information

Store below 110° F (43° C)

Inactive Ingredient

Water, Lavender (Lavandula angustifolia) Essential Oil, Fractionated Coconut (Cocos nucifera) Oil, Polysorbate 80, 2-Dimethylaminoethanol

Indications & Usage

Hand Sanitizer to reduce germs on skin

Otc - Questions

866-421-0309 or [email protected]

* Please review the disclaimer below.