71712-004 NDC - SANITIZINGSPRAY ()

Drug Information

Product NDC: 71712-004
Proprietary Name: SanitizingSpray
Non Proprietary Name:
Active Ingredient(s):
Administration Route(s):
Dosage Form(s):

Labeler Information

Field Name	Field Value
Labeler Name:	Wuxi Huoban Daily-Use Chemicals Science and Technology Co., Ltd
Product Type:
FDA Application Number:	part333A
Marketing Category:	OTC MONOGRAPH NOT FINAL
Start Marketing Date:	3/30/2020

Package Information

No.	Package Code	Package Description
1	71712-004-01	60 mL in 1 BOTTLE, SPRAY (71712-004-01)
2	71712-004-02	100 mL in 1 BOTTLE, SPRAY (71712-004-02)
3	71712-004-03	150 mL in 1 BOTTLE, SPRAY (71712-004-03)
4	71712-004-04	200 mL in 1 BOTTLE, SPRAY (71712-004-04)
5	71712-004-05	250 mL in 1 BOTTLE, SPRAY (71712-004-05)
6	71712-004-06	300 mL in 1 BOTTLE, SPRAY (71712-004-06)
7	71712-004-07	300 mL in 1 BOTTLE, SPRAY (71712-004-07)
8	71712-004-08	400 mL in 1 BOTTLE, SPRAY (71712-004-08)
9	71712-004-09	450 mL in 1 BOTTLE, SPRAY (71712-004-09)
10	71712-004-10	500 mL in 1 BOTTLE, SPRAY (71712-004-10)
11	71712-004-11	750 mL in 1 BOTTLE, SPRAY (71712-004-11)
12	71712-004-12	59 mL in 1 BOTTLE, SPRAY (71712-004-12)
13	71712-004-13	88 mL in 1 BOTTLE, SPRAY (71712-004-13)
14	71712-004-14	147 mL in 1 BOTTLE, SPRAY (71712-004-14)
15	71712-004-15	177 mL in 1 BOTTLE, SPRAY (71712-004-15)
16	71712-004-16	207 mL in 1 BOTTLE, SPRAY (71712-004-16)
17	71712-004-17	236 mL in 1 BOTTLE, SPRAY (71712-004-17)
18	71712-004-18	295 mL in 1 BOTTLE, SPRAY (71712-004-18)
19	71712-004-19	414 mL in 1 BOTTLE, SPRAY (71712-004-19)
20	71712-004-20	443 mL in 1 BOTTLE, SPRAY (71712-004-20)
21	71712-004-21	443 mL in 1 BOTTLE, SPRAY (71712-004-21)
22	71712-004-22	503 mL in 1 BOTTLE, SPRAY (71712-004-22)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	71712-004	The 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 NAME	SanitizingSpray	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX	80 v/v	A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
START MARKETING DATE	3/30/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	OTC MONOGRAPH NOT FINAL	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.
APPLICATION NUMBER	part333A	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.
LABELER NAME	Wuxi Huoban Daily-Use Chemicals Science and Technology Co., Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.

71712-004 NDC - SANITIZINGSPRAY ()

Drug Information

Labeler Information

Package Information

NDC Record

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