NDC 73635-1220 Salicylic Iodine (iodo Salicilico) First Aid Antiseptic

Iodine 2%

NDC Product Code 73635-1220

NDC 73635-1220-1

Package Description: 30 mL in 1 BOTTLE, WITH APPLICATOR

NDC Product Information

Salicylic Iodine (iodo Salicilico) First Aid Antiseptic with NDC 73635-1220 is a a human over the counter drug product labeled by Germa Products, Llc. The generic name of Salicylic Iodine (iodo Salicilico) First Aid Antiseptic is iodine 2%. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Germa Products, Llc

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.

Salicylic Iodine (iodo Salicilico) First Aid Antiseptic 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.

  • IODINE 20 mg/mL

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)
  • ALCOHOL (UNII: 3K9958V90M)

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: Germa Products, Llc
Labeler Code: 73635
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: 03-29-2021 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.

Salicylic Iodine (iodo Salicilico) First Aid Antiseptic Product Label Images

Salicylic Iodine (iodo Salicilico) First Aid Antiseptic 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

Iodine 2%


First aid antiseptic


As a first aid to help prevent skin infection in minor cuts, scrapes and burns


For external use only

Ask a doctor before use. if you have deep or puncture wounds, animal bites or serious burns. When using this product. do not use in eyes or apply over large areas of the body. do not use longer than 1 week unless directed by a doctor.

Stop use and ask a doctor if condition persists or gets worse

Ask A Doctor Before Use If

If you have deep or puncture wounds, animal bites or serious burns.

Keep Out Of Reach Of Children.

Keep out of the reach of children. If swallowed, get medical

help or contact a Poison Control Center right away.


Clean the affected area, apply a small amount on the area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.

Other Information

Product will stain skin and clothing.

Inactive Ingredients

Alcohol, salicylic acid, and water.

* Please review the disclaimer below.