APLIN SPOT ALL KILL- niacinamide cream

APLIN SPOT ALL KILL by

Drug Labeling and Warnings

APLIN SPOT ALL KILL by is a Otc medication manufactured, distributed, or labeled by Newizcompany. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

NIACINAMIDE

INACTIVE INGREDIENT

WATER, BUTYLENE GLYCOL, ARGININE, ALOE BARBADENSIS LEAF EXTRACT, GLYCERIN, ETC.

PURPOSE

Skin Protectant - Brightening

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Apply proper amount to the skin.

WARNINGS

Cautions :

1. When you use this product and find any of following problems, stop using it. if you keep using it despite the problem, the symptom will get worse, so you will have to go see a dermatologist.

(1) During use, if you have red spots, swelling, itching, or any other stimuli.

(2) if the applied region has any problem above for direct light.

2.Do not use the product on wound or dermatitis. 3.Attentive points for storage and treatment :

(1)Use il right after the opening.

(2)Do not use it around eye area.

(3)Store it in the place where infants or children cannot touch. (4)do not store it where it has either high or low temperature or there is direct light.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

APLIN SPOT ALL KILL 
niacinamide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71079-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA FLOWER (UNII: 575DY8C1ER)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71079-0001-1	50 mL in 1 JAR; Type 0: Not a Combination Product	09/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/01/2015

Labeler - Newizcompany (689851607)

Registrant - Newizcompany (689851607)

Establishment
Name	Address	ID/FEI	Business Operations
Newizcompany		689851607	manufacture(71079-0001)