76906-001 NDC - WET WIPE ()

Drug Information

  • Product NDC: 76906-001
  • Proprietary Name: Wet Wipe
  • Non Proprietary Name:
  • Active Ingredient(s): 70 g/100g ALCOHOL
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Zhejiang BeiTao Hygienic Products Co., Ltd.
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:3/21/2020
End Marketing Date:10/10/2020

Package Information

No. Package Code Package Description Billing Unit
176906-001-0110 POUCH in 1 BAG (76906-001-01) / 5 g in 1 POUCH
276906-001-0110 POUCH in 1 BAG (76906-001-01) / 5 g in 1 POUCH
376906-001-0220 POUCH in 1 BAG (76906-001-02) / 5 g in 1 POUCH
476906-001-0220 POUCH in 1 BAG (76906-001-02) / 6.5 g in 1 POUCH
576906-001-0325 POUCH in 1 BAG (76906-001-03) / 5 g in 1 POUCH
676906-001-0325 POUCH in 1 BOX (76906-001-03) / 7.2 g in 1 POUCH
776906-001-0450 POUCH in 1 BAG (76906-001-04) / 5 g in 1 POUCH
876906-001-0450 POUCH in 1 BAG (76906-001-04) / 6 g in 1 POUCH
976906-001-05350 POUCH in 1 BAG (76906-001-05) / 5 g in 1 POUCH
1076906-001-05350 POUCH in 1 BAG (76906-001-05) / 5.8 g in 1 POUCH
1176906-001-0680 POUCH in 1 BAG (76906-001-06) / 5 g in 1 POUCH
1276906-001-0680 POUCH in 1 BAG (76906-001-06) / 5.25 g in 1 POUCH
1376906-001-07100 POUCH in 1 BAG (76906-001-07) / 5 g in 1 POUCH
1476906-001-07100 POUCH in 1 BOX (76906-001-07) / 4.8 g in 1 POUCH
1576906-001-08135 POUCH in 1 BAG (76906-001-08) / 5 g in 1 POUCH
1676906-001-08135 POUCH in 1 PAIL (76906-001-08) / 2.07 g in 1 POUCH
1776906-001-09250 POUCH in 1 BAG (76906-001-09) / 5 g in 1 POUCH
1876906-001-09250 POUCH in 1 PAIL (76906-001-09) / 2.08 g in 1 POUCH
1976906-001-1060 POUCH in 1 BAG (76906-001-10) / 5.83 g in 1 POUCH
2076906-001-1125 POUCH in 1 BAG (76906-001-11) / 7.2 g in 1 POUCH
2176906-001-12100 POUCH in 1 BAG (76906-001-12) / 4.8 g in 1 POUCH
2276906-001-1310 POUCH in 1 BAG (76906-001-13) / 5 g in 1 POUCH
2376906-001-1310 g in 1 BAG (76906-001-13)

NDC Record

Field Name Field Value Definition
PRODUCT NDC76906-001The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEWet WipeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/21/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALProduct 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.
APPLICATION NUMBERpart333AThis 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.
LABELER NAMEZhejiang BeiTao Hygienic Products Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC76906-001The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEWet WipeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/4/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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.
APPLICATION NUMBERM003This 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.
LABELER NAMEZhejiang BeiTao Hygienic Products Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/21/2025

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