FOSTER AND THRIVE POVIDONE-IODINE- povidone iodine liquid

Foster and Thrive Povidone-Iodine by

Drug Labeling and Warnings

Foster and Thrive Povidone-Iodine by is a Otc medication manufactured, distributed, or labeled by Strategic Sourcing Services, LLC, Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Foster & Thrive Povidone-Iodine

Drug Facts

Active Ingredient

Povidone-Iodine 10% (1% Available iodine)

Purpose

First Aid Antiseptic

Uses

First aid to help prevent infection in in minor: cuts, scrapes and burns.

Warnings

For external use only

Do not use

in the eyes. Over large areas of the body.

Ask a doctor before use

in case of deep or puncture wounds, animal bites, or serious burns.

Stop use and consult a doctor if:

The condition persists or gets worse. Need to use this product for more than 1 week.

Keep out of reach of children.

• If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Clean the affected area. Apply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let dry first.

Inactive Ingredient

Citric acid, Dibasic sodium Phosphate, Glycerin, Nonoxynol-9, Purified water, sodium hydroxide.

QUESTIONS

Questions? Call 833-358-6431

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FOSTER AND THRIVE POVIDONE-IODINE 
povidone iodine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70677-1208
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
GLYCERIN (UNII: PDC6A3C0OX)
NONOXYNOL-9 (UNII: 48Q180SH9T)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70677-1208-1	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/07/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	10/07/2024

Labeler - Strategic Sourcing Services, LLC (116956644)

Registrant - Pharma Nobis, LLC (118564114)

Establishment
Name	Address	ID/FEI	Business Operations
Pharma Nobis, LLC		118564114	analysis(70677-1208) , manufacture(70677-1208) , pack(70677-1208) , label(70677-1208)