ALCOHOL PREP PAD- isopropyl alcohol swab

Alcohol Prep Pad by

Drug Labeling and Warnings

Alcohol Prep Pad by is a Otc medication manufactured, distributed, or labeled by Shandong Haiyan Medical Manufacture Co., Ltd., Shandong Haiyan Medical Manufacture Co., Ltd. . Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl Alcohol 70%v/v

Purpose

Antiseptic

Use

For preparation of skin prior to injection.

WARNINGS

For External use only.

Flammable,keep away from fire or flame.

Do not use with electrocautery procedures in eyes.

Stop use and ask a doctor if irritation and redness develop,condition persists for more than 72 hours .

keep out of reach of children

In case of accidental ingestion, seek professional assistance or consult a PoisonControl Center immediately.

Directions

Wipe injection site vigorously and discard.

Inactive ingredients

purified water

PRINCIPAL DISPLAY PANEL

section text here

INGREDIENTS AND APPEARANCE

ALCOHOL PREP PAD 
isopropyl alcohol swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42339-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	0.7 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42339-001-01	15 in 1 CONTAINER	12/01/2017
1		200 in 1 BOX; Type 0: Not a Combination Product
2	NDC: 42339-001-04	100 in 1 CONTAINER	12/01/2017
2		50 in 1 BOX; Type 0: Not a Combination Product
3	NDC: 42339-001-02	100 in 1 CONTAINER	12/01/2017
3		100 in 1 BOX; Type 0: Not a Combination Product
4	NDC: 42339-001-03	3000 in 1 CONTAINER; Type 0: Not a Combination Product	12/01/2017
5	NDC: 42339-001-05	30 in 1 CASE	12/01/2017
5		36 in 1 BOX; Type 0: Not a Combination Product
6	NDC: 42339-001-06	24 in 1 CASE	12/01/2017
6		50 in 1 BOX; Type 0: Not a Combination Product
7	NDC: 42339-001-07	24 in 1 CASE	12/01/2017
7		100 in 1 BOX; Type 0: Not a Combination Product
8	NDC: 42339-001-08	20 in 1 CASE	12/01/2017
8		140 in 1 BOX; Type 0: Not a Combination Product
9	NDC: 42339-001-09	30 in 1 CASE	12/01/2017
9		100 in 1 BOX; Type 0: Not a Combination Product
10	NDC: 42339-001-10	15 in 1 CASE	12/01/2017
10		200 in 1 BOX; Type 0: Not a Combination Product
11	NDC: 42339-001-11	20 in 1 CASE	12/01/2017
11		200 in 1 BOX; Type 0: Not a Combination Product
12	NDC: 42339-001-12	12 in 1 CASE	12/01/2017
12		100 in 1 BOX; Type 0: Not a Combination Product
13	NDC: 42339-001-13	48 in 1 CASE	12/01/2017
13		200 in 1 BOX; Type 0: Not a Combination Product
14	NDC: 42339-001-14	20 in 1 CASE	12/01/2017
14		200 in 1 BOX; Type 0: Not a Combination Product
15	NDC: 42339-001-15	24 in 1 CASE	12/01/2017
15		400 in 1 BOX; Type 0: Not a Combination Product
16	NDC: 42339-001-16	20 in 1 CASE	12/01/2017
16		50 in 1 BOX; Type 0: Not a Combination Product
17	NDC: 42339-001-17	20 in 1 CASE	12/01/2017
17		200 in 1 BOX; Type 0: Not a Combination Product
18	NDC: 42339-001-18	4 in 1 CASE	12/01/2017
18		1000 in 1 BOX; Type 0: Not a Combination Product
19	NDC: 42339-001-19	20 in 1 CASE	12/01/2017
19		200 in 1 BOX; Type 0: Not a Combination Product
20	NDC: 42339-001-20	10 in 1 CASE	12/01/2017
20		100 in 1 BOX; Type 0: Not a Combination Product
21	NDC: 42339-001-21	30 in 1 CASE	12/01/2017
21		36 in 1 BOX; Type 0: Not a Combination Product
22	NDC: 42339-001-22	20 in 1 CASE	12/01/2017
22		80 in 1 BOX; Type 0: Not a Combination Product
23	NDC: 42339-001-23	15 in 1 CASE	12/01/2017
23		120 in 1 BOX; Type 0: Not a Combination Product
24	NDC: 42339-001-24	20 in 1 CASE	12/01/2017
24		100 in 1 BOX; Type 0: Not a Combination Product
25	NDC: 42339-001-25	30 in 1 CASE	12/01/2017
25		100 in 1 BOX; Type 0: Not a Combination Product
26	NDC: 42339-001-26	30 in 1 CASE	12/01/2017
26		140 in 1 BOX; Type 0: Not a Combination Product
27	NDC: 42339-001-27	30 in 1 CASE	12/01/2017
27		200 in 1 BOX; Type 0: Not a Combination Product
28	NDC: 42339-001-28	96 in 1 CASE	12/01/2017
28		100 in 1 BOX; Type 0: Not a Combination Product
29	NDC: 42339-001-29	10 in 1 CASE	12/01/2017
29		100 in 1 BOX; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part344	02/18/2012

Labeler - Shandong Haiyan Medical Manufacture Co., Ltd. (421283439)

Establishment
Name	Address	ID/FEI	Business Operations
Shandong Haiyan Medical Manufacture Co., Ltd.		421283439	manufacture(42339-001)