EQUATE FIRST AID ANTISEPTIC- povidone-iodine solution

equate First Aid Antiseptic by

Drug Labeling and Warnings

equate First Aid Antiseptic by is a Otc medication manufactured, distributed, or labeled by Walmart Inc., Lights Medical Manufacture Co., Ltd., Lights Medical Manufacture Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Povidone-Iodine USP (10%)

(1% available Iodine)

PURPOSE

Purpose: First Aid Antiseptic

INDICATIONS & USAGE

Use:

First aid antiseptic to help prevent the risk of infection in minor cuts, scrapes and burns.

WARNINGS

Warnings:

For external use only

Do not use

• to the eyes or over large areas of the body
• longer than a week unless directed by a doctor 

ASK DOCTOR

Ask a doctor before use in case of deep or puncture wounds, animal bites, or serious burns

Stop use and ask a doctor if condition persists or gets worse

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or consult a poison control center right away

Directions

• clean the affacted area,
• apply a small anount of the product to the area 1-3 times daily.
• maybe covered with a sterile bandage.
• if bandaged, let dry first.

OTHER SAFETY INFORMATION

Other information

• Store between 15-30C (59-86F)

INACTIVE INGREDIENT

Inactive Ingredient

Citric acid, disodium hydrogen phosphate, purified water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EQUATE FIRST AID ANTISEPTIC 
povidone-iodine solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-230
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4)	IODINE	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79903-230-08	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/10/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	10/10/2023

Labeler - Walmart Inc. (051957769)

Registrant - Lights Medical Manufacture Co., Ltd. (529128649)

Establishment
Name	Address	ID/FEI	Business Operations
Lights Medical Manufacture Co., Ltd.		529128649	manufacture(79903-230)