BABY WIPES WITH ALLANTOIN- allantoin liquid

Baby Wipes with Allantoin by

Drug Labeling and Warnings

Baby Wipes with Allantoin by is a Otc medication manufactured, distributed, or labeled by Yinjing Medical Technology (Shanghai) Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Baby Wipes with Allantoin

ACTIVE INGREDIENT

Allantoin 0.5%(w/w)

Skin Protectant

Uses:

Temporarily protects and helps relieve minor skin irritations

Warnings:

For external use only.

When using this product, do not get into eyes.

Stop use and ask a doctor if the rash persists for more than 7 days,
or tends to reoccur. Keep out of reach of children

Stop use and ask a doctor

if rash persists for more than 7 days, or tends to reoccur.

Keep out of reach of children.

Directions

• Open lid, remove tab ans pull wipe through
•  Take wipe and rub thoroughly over the affected area
  
• Use as many wipes as needed
  
• DO NOT FLUSH,dispose of used wipes in trash

Inactive Ingredients:

Water, Propylene Glycol, Polysorbate-20, Chamomilla Recutita Water, Tocopheryl acetate, Benzalkonium chloride, Aloe barbadensis leaf juice, potassium sorbate, Sodium Benzoate, Gluconolactone.

Other Information:

Store in a cool dry place

Baby Wipes with Allantion 80 Count (

44019-400-80)

INGREDIENTS AND APPEARANCE

BABY WIPES WITH ALLANTOIN 
allantoin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44019-400
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
GLUCONOLACTONE (UNII: WQ29KQ9POT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44019-400-80	360 g in 1 BAG; Type 0: Not a Combination Product	08/03/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	08/03/2016

Labeler - Yinjing Medical Technology (Shanghai) Co., Ltd. (530501535)