NASAL DRYNESS RELIEF GEL- allantoin gel

Nasal Dryness Relief Gel by

Drug Labeling and Warnings

Nasal Dryness Relief Gel by is a Otc medication manufactured, distributed, or labeled by Genuine Virgin Aloe Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Allantoin 0.5%

Purpose

Skin Protectant

Uses

• Temporarily protects and helps relieve chapped or cracked skin
• Helps protect from the drying effects of wind and cold weather

Warnings

For external use only.

Don not use

• on deep puncture wounds
• on infection
• on lacerations

When using this product

do not get into eyes

Stop use and ask a doctor if

condition worsens or does not improve within 7 days.

Keep out of reach of children.

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

Directions

Apply a thin layer to external nasal passages area(s) as often as needed. May also be used on other facial areas to help relieve disconfort.

For CPAP mask users: Before each use, apply a thin layer to nasal area and wherever mask touches the skin. After each use, apply gel to mask lines to replenish moisture and revitalize skin.

Other information

• Store at room temperature

Questions?

1-800-279-7282 M-F 8am-4pm PST

Inactive Ingredients

water, aloe barbadensis (aloe vera) leaf juice*, carbomer, arginine, ethylhexylglycerin, phenoxyethanol.

*Certified Organic Ingredient - Mayacert Certifier

Indications & Usage Section

Temporarily protects and helps relieve chapped or cracked skin * Helps protect from the drying effects of wind and cold weather

Labels

Nasal Dryness Relief_1oz_label

INGREDIENTS AND APPEARANCE

NASAL DRYNESS RELIEF GEL 
allantoin gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10738-051
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ARGININE (UNII: 94ZLA3W45F)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CARBOMER 934 (UNII: Z135WT9208)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10738-051-10	1 in 1 CARTON	05/20/2022
1	NDC: 10738-051-15	28 g in 1 TUBE; 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)	05/20/2022

Labeler - Genuine Virgin Aloe Corporation (961374147)

Establishment
Name	Address	ID/FEI	Business Operations
Genuine Virgin Aloe Corporation		961374147	manufacture(10738-051)