NDC 72663-130 Welly Human Repair Kit

Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, Hydrocortisone, Alcohol

NDC Product Code 72663-130

NDC Code: 72663-130

Proprietary Name: Welly Human Repair Kit Additional informationCallout TooltipWhat 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: Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, Hydrocortisone, Alcohol Additional informationCallout TooltipWhat 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.


Code Structure
  • 72663 - Welly Health Pbc
    • 72663-130 - Welly Human Repair Kit

NDC 72663-130-23

Package Description: 1 KIT in 1 KIT * .9 mL in 1 POUCH * .9 mL in 1 POUCH * .5 mL in 1 POUCH

NDC Product Information

Welly Human Repair Kit with NDC 72663-130 is a a human over the counter drug product labeled by Welly Health Pbc. The generic name of Welly Human Repair Kit is bacitracin zinc, neomycin sulfate, polymyxin b sulfate, hydrocortisone, alcohol. The product's dosage form is kit and is administered via form.

Labeler Name: Welly Health Pbc

Dosage Form: Kit - A packaged collection of related material.

Product Type: Human Otc Drug Additional informationCallout TooltipWhat 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)

Additional informationCallout TooltipAbout 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.

  • PETROLATUM (UNII: 4T6H12BN9U)
  • ALCOHOL (UNII: 3K9958V90M)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • PARAFFIN (UNII: I9O0E3H2ZE)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • WATER (UNII: 059QF0KO0R)
  • WHITE WAX (UNII: 7G1J5DA97F)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
  • D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
  • D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
  • WATER (UNII: 059QF0KO0R)
  • TROLAMINE (UNII: 9O3K93S3TK)

Product Labeler Information

Additional informationCallout TooltipWhat is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

* Please review the disclaimer below.

Welly Human Repair Kit Product Label Images

Welly Human Repair Kit 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

Triple Antibiotic Ointment

Drug Facts

Active Ingredient (In Each Gram)

Bacitracin zinc 400 unitsNeomycin sulfate (3.5mg Neomycin)Polymyxin B sulfate 5000 units

Purpose

First Aid Antibiotics

Anti-itch

Antiseptic

Uses

First aid to help prevent infection in minor cuts, scrapes and burns

  • For temporary relief of itching associated with minor skin irritations, inflammation, or rashes.Other uses of product should be only under the advice and supervision of a doctor.

Warnings

  • For external use onlyDo not useinternallyin eyesover large areas of the body or on puncture wounds, animal bites or serious burnsfor more than 1 week unless directed by a doctorif you are allergic to any of the ingredientsStop use and ask a doctor ifa rash or other allergic reaction developscondition worsens or persists

  • For external use onlyDo not usein eyesfor treatment of diaper rashfor feminine itchingStop use, ask a doctorif condition worsens or lasts more than 7 days, or clears up and occurs again within a few dayswith use of other hydrocortisone products

For external use onlyFlammable, keep away from fire or flame.Do not use in eyes, if this happens, rinse thoroughly with water.Stop use, ask a doctor if, irritation develops and persists for 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If ingested, contact a Poison Control Center right away.

Keep out of reach of children. If ingested, contact a Poison Control Center right away

Keep out of reach of children. If ingested, get medical help or contact a Poison Control Center right away.

Directions

  • Clean affected areaapply a small amount 1 to 3 times dailymay cover with a sterile bandage

  • Apply to affected area not more than 3 to 4 times dailychildren under 2: ask a doctor

  • Wet hands & wrists thoroughly with product and allow to dry without wiping

Inactive Ingredients

Petrolatum

Emulsifying wax, ethanol, methylparaben, mineral oil, paraffin, petrolatum, propylparaben, purified water, white wax

Aloe vera, carbomer, D&C green #5, D&C yellow #10, fragrance, purified water, triethanolamine

1% Hydrocortisone Cream

Drug Facts

Active Ingredient

Hydrocortisone 1.0%

Ethyl Alcohol 66.5%

Instant Hand Sanitizer Gel

Drug Facts

Use

For handwashing to decrease bacteria on skin without soap and water.

* Please review the disclaimer below.

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