DOCTOR INKS IPA WIPES- isopropyl alcohol cloth

Drug Labeling and Warnings

Drug Details [pdf]

DRUG FACTS:

ACTIVE INGREDIENT:

Isopropyl Alcohol 70%

PURPOSE:

Antiseptic

USES:

Skin preparation Antiseptic/Sanitizer to help reduce bacteria that may cause infection pre new tattoo and piercings.

DIRECTIONS FOR USE:

Wipe liberally over the skin, single use only
Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENTS:

Chlorphenesin, Purified Water, Propylene Glycol

WARNINGS:

FLAMMABLE. Keep away from fire, electrical & spark
For external use only. Do not use In ears, eyes or mouth.

 When using this product do not use in or near the eyes.
 In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs.

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

QUESTIONS?

+1(888) 331-8332, Mon-Fri 9:00AM-5:00PM (EST)

SPL UNCLASSIFIED SECTION

Kills 99.9% of Common Germs

SEE BACK PANEL FOR PRECAUTIONARY STATEMENTS AND FIRST AID

DO NOT FLUSH

40 GSM Spunlace

100% Lint free

Individual foil sachet
packaged single use
70% IPA saturate wipes

Thicker stronger 40gsm fabric

Extended shelf life

FORMULATED IN THE USA
MADE IN CHINA

​ESC BRANDS

DISTRIBUTED BY: ESC BRANDS, LLC.
1026 BLUE PRINCE ROAD, SUITE B
BLUEFIELD, WV 24701
Email: info@escbrands.com

www.escbrands.com

SATURATED WITH 70% ISOPROPYL ALCOHOL

Packaging

INGREDIENTS AND APPEARANCE

DOCTOR INKS IPA WIPES 
isopropyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71884-205
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CHLORPHENESIN (UNII: I670DAL4SZ)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71884-205-01	100 in 1 BOX	05/01/2026
1		1 in 1 PACKET
1		0.244 mL in 1 PACKAGE; Type 0: Not a Combination Product
2	NDC: 71884-205-02	50 in 1 PACKET	05/01/2026
2		2.459 mL in 1 PACKAGE; Type 0: Not a Combination Product
3	NDC: 71884-205-03	80 in 1 CONTAINER	05/01/2026
3		2.635 mL in 1 PACKAGE; Type 0: Not a Combination Product
4	NDC: 71884-205-04	120 in 1 PACKET	05/01/2026
4		2.635 mL in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/01/2026

Labeler - Enviro Specialty Chemicals Inc (202621850)