HAND SANITIZER, NAMASTE- alcohol gel

Land: USA

Språk: engelsk

Kilde: NLM (National Library of Medicine)

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Last ned Preparatomtale (SPC)
29-11-2022

Aktiv ingrediens:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Tilgjengelig fra:

Merci Handy Corporation

Administreringsrute:

TOPICAL

Resept typen:

OTC DRUG

Indikasjoner:

for handwashing to decrease bacteria on the skin

Autorisasjon status:

OTC monograph not final

Preparatomtale

                                HAND SANITIZER, NAMASTE- ALCOHOL GEL
MERCI HANDY CORPORATION
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may_
_be marketed if they comply with applicable regulations and policies.
FDA has not_
_evaluated whether this product complies._
----------
HAND SANITIZER, NAMASTE
_DRUG FACTS_
_ACTIVE INGREDIENT_
Alcohol 67%
_PURPOSE_
Antiseptic
_USE_
for handwashing to decrease bacteria on the skin
_WARNINGS_
FOR EXTERNAL USE ONLY.
Flammable, keep away from fire or flame.
DO NOT USE
in the eyes. In case of contact, flush eyes with water.
STOP USE AND ASK A DOCTOR IF
irritation and redness develop
condition persists for more than 72 hours
KEEP OUT OF REACH OF CHILDREN.
If swallowed, get medical help or contact a Poison Control Center
right away.
_DIRECTIONS_
wet hands thoroughly with product and allow to dry without wiping
_OTHER INFORMATION_
store at a temperature below 110° F (43° C)
_INACTIVE INGREDIENTS_
Water (Aqua), Fragrance (Parfum), Aloe Vera Leaf Juice Powder,
Glycerin, Propylene
Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl
Propanol,
Mannitol, Microcrystalline Cellulose, Sucrose, Corn (Zea Mays) Starch,
Denatonium
Benzoate, Tocopheryl Acetate, Maltodextrin, Hydroxypropyl
Methylcellulose, Potassium
Sorbate, Sodium Benzoate, Hexyl Cinnamal, Benzyl Benzoate, Linalool,
imonene,
Ferric Ferrocyanide, D&C Red No. 33, D&C Red No. 30, FD&C Blue No. 1.
QUESTIONS OR COMMENTS?
(646)-358-3432
PACKAGE LABELING:
HAND SANITIZER, NAMASTE
alcohol gel
PRODUCT INFORMATION
PRODUCT TYPE
HUMAN OTC DRUG
ITEM CODE (SOURCE)
NDC:72866-002
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRENGTH
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
ALCOHOL
670 mg in 1 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRENGTH
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
MANNITOL (UNII: 3OWL53L36A)
MICROCRYSTALLINE CELLULOSE (UNII
                                
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