NDC 74149-042 Air And Water Christmas Berry Hand Sanitizer

Alcohol Liquid Topical

NDC Product Information

Air And Water Christmas Berry Hand Sanitizer with NDC 74149-042 is a human over the counter drug product labeled by Yiwu Yangjie Daily Chemicals Co.,ltd.. The generic name of Air And Water Christmas Berry Hand Sanitizer is alcohol. The product's dosage form is liquid and is administered via topical form.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Air And Water Christmas Berry Hand Sanitizer 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.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:

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: Yiwu Yangjie Daily Chemicals Co.,ltd.
Labeler Code: 74149
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 10-16-2020 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.

Air And Water Christmas Berry Hand Sanitizer Product Label Images

Air And Water Christmas Berry Hand Sanitizer 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               Ethyl Alcohol       ...........         70% v/v

Otc - Purpose


Otc - Keep Out Of Reach Of Children

If swallowed, get medical help or contact a poison control center right away.

Indications & Usage

  • To decrease bacteria on the skin that could cause diseaseWhen water, soap and towel are not available. recommended for repeated use


  • For external use onlyFlammable. Keep away from fire or flame.When using this product Keep out of eyes, ears or mouth In case of eye contact, flush eyes with water.Avoid contact with broken skin.Do not inhale or ingestStop use and ask a doctor If Redness or irritation develops.Condition persists for more than 72 hoursOther information:Store under 105℉ (40℃).May discolor certain fabrics.Harmful to wood finishes and plastics.


  • Wet hands thoroughly with product and allow to dry without wiping.No rinsing required.For children under 6, use only under adult supervision.Not recommended for infants.

Inactive Ingredient

Water (Aqua), Triethanolamine, Carbomer, Aloe Bardadensis Leaf Extract, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E). Main Contain: FD & C Red 40 (Cl 16035), FD & C Yellow 6 (Cl 15985), FD& C Violet 2 (Cl 60725), FD& C Blue 1 (Cl 42090), FD & C Yellow 5 (Cl 19140), FD& C Red 33 (Cl 17200).

* Please review the disclaimer below.