国家: 美国
语言: 英文
来源: NLM (National Library of Medicine)
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
Creative Essences
TOPICAL
OTC DRUG
Antiseptic, Hand Sanitizer Hand Sanitizer to help reduce bacteria that potentially can cause disease. Recommended for repeated use. - in children less than 2 months of age - on open skin wounds Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
OTC monograph not final
HAND SANITIZER- ALCOHOL GEL CREATIVE ESSENCES _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._ ---------- FRESH NECTAR HAND SANITIZER 2 FL OZ ACTIVE INGREDIENT(S) Alcohol 80% v/v. Purpose: Antiseptic PURPOS E Antiseptic, Hand Sanitizer US E Hand Sanitizer to help reduce bacteria that potentially can cause disease. Recommended for repeated use. WARNINGS For external use only. Flammable. Keep away from heat or flame DO NOT USE in children less than 2 months of age on open skin wounds When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition. Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. DIRECTIONS Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing. OTHER INFORMATION Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F) INACTIVE INGREDIENTS Aloe vera extract, aminomethylpropanol, carbomer, cyclomethicone 5, fragrance, 3-o-ethyl ascrobic acid, vitamin e acetate, water PACKAGE LABEL - PRINCIPAL DISPLAY PANEL 60 mL NDC: 70658-124-31 HAND SANITIZER alcohol gel PRODUCT INFORMATION PRODUCT T YPE HUMAN OTC DRUG ITE M CODE (SOURCE ) NDC:70 6 58 -124 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M) ALCOHOL 8 0 mL in 10 0 mL INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH 3 -O -ETHYL ASCO RBIC ACID (UNII: 6 MW6 0 CB71P) 0 .0 2 g in 10 0 mL AMINO METHYLPRO PANO L (UNII: LU49 E6 6 26 Q) 0 阅读完整的文件