NDC 61312-003 Wet Wipes

NDC Product Code 61312-003

NDC CODE: 61312-003

Proprietary Name: Wet Wipes 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.

NDC Code Structure

  • 61312 - Hangzhou Guoguang Touring Commodity Co., Ltd.

NDC 61312-003-01

Package Description: 35 POUCH in 1 BAG > .0054 g in 1 POUCH

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

NDC Product Information

Wet Wipes with NDC 61312-003 is a product labeled by Hangzhou Guoguang Touring Commodity Co., Ltd.. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 797892.

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • DODECYL PROPIONATE (UNII: 7G537BMD9L)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • HEXYLENE GLYCOL (UNII: KEH0A3F75J)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • SODIUM LAURAMINOPROPIONATE (UNII: X5NJA9HXPU)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • TEA LEAF OIL (UNII: VC855RRT77)
  • CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
  • DMDM HYDANTOIN (UNII: BYR0546TOW)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • PEG-40 HYDROGENATED LANOLIN (UNII: 959P5CXE48)
  • TOCOPHERYL RETINOATE (UNII: 0WN694NBMM)
  • DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
  • IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Hangzhou Guoguang Touring Commodity Co., Ltd.
Labeler Code: 61312
Start Marketing Date: 02-25-2015 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 - INACTIVATED, the listing data was inactivated by the FDA. 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.

Information for Patients

Salicylic Acid Topical

Salicylic Acid Topical is pronounced as (sal'' i sil' ik as' id)

Why is salicylic acid topical medication prescribed?
Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions ...
[Read More]

* Please review the disclaimer below.

Wet Wipes Product Label Images

Wet Wipes 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

Salicylic acid 2%

Purpose

Acne treatment

Use

For the treatment of acne

Warnings

For external use only


when using this product


with other topical acne medications ,at the same time or immediately afterwards ,increased skin dryness ,redness or


irritation may occur .If this happens ,only one medication should be used unless directed by a doctor.


avoid contact with eyes .if contact occurs, rinse thoroughly with water. keep away from mouth and lips.


stop use and ask doctor if skin irritation occurs.


Keep out of reach of children ,If swallowed ,get medical help or contact a Poison Control Center immediately.

Keep Out Of Reach Of Children

Keep out of reach of children ,If swallowed ,get medical help or contact a Poison Control Center immediately.

Directions

Cleanse skin thoroughly before applying medication ,remove wipe ,unfold and wipe over entire affected area.


reseal label on package to maintain freshness.

Inactive Ingredient

Aqua (water),glycerin, propylene glycol , dodecyl polyglucoside, polysorbate 20,HEXYLENE GLYCOL , BENZYL ALCOHOL ,SODIUM LAURAMINOPROPIONATE ,ALOE BARBADENSIS(ALOE VERA )EXTRACT ,WHITE TEA EXTRACT ,CHAMOMILLA RECUTITA(CHAMOMILE)EXTRACT ,GLYDANT DMDM H,PHENOXYETHANOL ,PEG-40 HYDROGENATED CASTOR OIL,TOCOPHERYL ACETATE(VITAMIN E) ,DISODIUM EDTA,IODOPROPYNYL BUTYLCARBAMATE

* Please review the disclaimer below.