Страна: США
мова: англійська
Джерело: NLM (National Library of Medicine)
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)
Pop Fizz Designs
TOPICAL
OTC DRUG
OTC monograph not final
ALCOHOL- ALCOHOL GEL ALCOHOL- ALCOHOL LIQUID POP FIZZ DESIGNS _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._ ---------- SANITIZER GEL DRUG FACTS ACTIVE INGREDIENT Ethyl Alcohol 62% PURPOSE Antiseptic USES To help reduce bacteria on the skin. WARNINGS For external use only. Flammable. Keep away from fire or flame. Stop use and ask doctor if irritation or rash appears. KEEP OUT OF THE REACH OF CHILDREN If swallowed, get medical help. DIRECTIONS Pump as needed into the palm of hands. Rub hands together quickly until dry. Children under 6 years old should be supervised when using this product. OTHER INFORMATION Store below 118°F INACTIVE INGREDIENTS Water, Aloe Barbendensis Leaf Juice, Maltodextrin, Glycerin, Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethonoamine, Fragrance, FD&C Blue No. 1, D&C Red No. 33. ALCOHOL alcohol gel PRODUCT INFORMATION PRODUCT TYPE HUMAN OTC DRUG ITEM CODE (SOURCE) NDC:73884-002 ROUTE OF ADMINISTRATION TOPICAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRENGTH ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL INACTIVE INGREDIENTS INGREDIENT NAME STRENGTH GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) MALTODEXTRIN (UNII: 7CVR7L4A2D) ALOE VERA LEAF (UNII: ZY81Z83H0X) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) TROLAMINE (UNII: 9O3K93S3TK) PACKAGING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:73884-002- 12 10 in 1 BOX 09/20/2022 1 NDC:73884-002- 02 29 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:73884-002- 13 10 in 1 BOX 09/20/2022 2 NDC:73884-002- 03 29 mL in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:73884-002- 14 10 in 1 BOX 09/20/2022 3 NDC:73884-002- 04 2 Прочитайте повний документ