75749-052 NDC - HAND SANITIZER ()

Drug Information

Product NDC: 75749-052

Proprietary Name: HAND SANITIZER

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: NINGBO PRETTY TOURISM MANUFACTURE CO.,LTD.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/2/2020

Package Information

No. Package Code Package Description Billing Unit
175749-052-0130 mL in 1 BOTTLE, PLASTIC (75749-052-01)
275749-052-0250 mL in 1 BOTTLE, PLASTIC (75749-052-02)
375749-052-0354 mL in 1 BOTTLE, PLASTIC (75749-052-03)
475749-052-0460 mL in 1 BOTTLE, PLASTIC (75749-052-04)
575749-052-0580 mL in 1 BOTTLE, PLASTIC (75749-052-05)
675749-052-06100 mL in 1 BOTTLE, PLASTIC (75749-052-06)
775749-052-07150 mL in 1 BOTTLE, PLASTIC (75749-052-07)
875749-052-08250 mL in 1 BOTTLE, PLASTIC (75749-052-08)
975749-052-09300 mL in 1 BOTTLE, PLASTIC (75749-052-09)
1075749-052-10500 mL in 1 BOTTLE, PLASTIC (75749-052-10)
1175749-052-115 mL in 1 BOTTLE, SPRAY (75749-052-11)
1275749-052-1210 mL in 1 BOTTLE, SPRAY (75749-052-12)
1375749-052-1315 mL in 1 BOTTLE, SPRAY (75749-052-13)
1475749-052-1420 mL in 1 BOTTLE, SPRAY (75749-052-14)
1575749-052-1530 mL in 1 BOTTLE, SPRAY (75749-052-15)
1675749-052-1650 mL in 1 BOTTLE, SPRAY (75749-052-16)
1775749-052-1760 mL in 1 BOTTLE, SPRAY (75749-052-17)
1875749-052-18100 mL in 1 BOTTLE, SPRAY (75749-052-18)
1975749-052-19150 mL in 1 BOTTLE, SPRAY (75749-052-19)
2075749-052-20250 mL in 1 BOTTLE, SPRAY (75749-052-20)
2175749-052-21300 mL in 1 BOTTLE, SPRAY (75749-052-21)
2275749-052-22500 mL in 1 BOTTLE, SPRAY (75749-052-22)
2375749-052-23150 mL in 1 BOTTLE, PUMP (75749-052-23)
2475749-052-24237 mL in 1 BOTTLE, PUMP (75749-052-24)
2575749-052-25250 mL in 1 BOTTLE, PUMP (75749-052-25)
2675749-052-26300 mL in 1 BOTTLE, PUMP (75749-052-26)
2775749-052-27350 mL in 1 BOTTLE, PUMP (75749-052-27)
2875749-052-28473 mL in 1 BOTTLE, PUMP (75749-052-28)
2975749-052-29500 mL in 1 BOTTLE, PUMP (75749-052-29)
3075749-052-30750 mL in 1 BOTTLE, PUMP (75749-052-30)
3175749-052-311000 mL in 1 BOTTLE, PUMP (75749-052-31)
3275749-052-322000 mL in 1 BOTTLE, PUMP (75749-052-32)
3375749-052-332500 mL in 1 BOTTLE, PUMP (75749-052-33)
3475749-052-343000 mL in 1 BOTTLE, PUMP (75749-052-34)
3575749-052-354000 mL in 1 BOTTLE, PUMP (75749-052-35)
3675749-052-365000 mL in 1 BOTTLE, PUMP (75749-052-36)
3775749-052-3710000 mL in 1 BOTTLE, PUMP (75749-052-37)
3875749-052-3830 mL in 1 TUBE (75749-052-38)
3975749-052-3960 mL in 1 TUBE (75749-052-39)
4075749-052-4080 mL in 1 TUBE (75749-052-40)
4175749-052-41100 mL in 1 TUBE (75749-052-41)
4275749-052-42120 mL in 1 TUBE (75749-052-42)
4375749-052-43150 mL in 1 TUBE (75749-052-43)
4475749-052-44180 mL in 1 TUBE (75749-052-44)
4575749-052-45200 mL in 1 TUBE (75749-052-45)
4675749-052-46250 mL in 1 TUBE (75749-052-46)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75749-052The 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 NAMEHAND SANITIZERThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/2/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENINGBO PRETTY TOURISM MANUFACTURE 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: 2/1/2023