CORETEX ANTIBACTERIAL HAND SANITIZER- sd alcohol liquid

CoreTex Antibacterial Hand Sanitizer by

Drug Labeling and Warnings

CoreTex Antibacterial Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by CoreTex Products Inc, HealthSpecialty. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

SD Alcohol 40-B 62.5%

Purpose

Antimicrobial

Uses

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

Flammable. Keep away from heat or flame.

For external use only.

When using this product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or rash appears and lasts.

Keep out of reach of children. If swallowed, get help or contact a Poison Control Center right away.

Directions

Put enough product in your palm to cover hands and rub hands together briskly until dry.

Inactive Ingredients

actinidia chinesis (kiwi) extract, aloe barbadenis leaf juice, aminomethyl propanol, brassica oleracea italica (broccoli) extract, cannabis sativa (hemp) seed extract, carbomer citrullus vulgaris (watermelon) fruit extract, euterpe oleracea fruit extract, fragaria vesca (strawberry) fruit extract, glycerin, helianthus annus (sunfloer) seed oil, hippophae rhamnoides (sea buckthorn) fruit extract, lycium barbarum (goji) extract, myrciaria dubia (camu camu) fruit extract, propanediol, propylene glycol, punica granatum extract, rubus idaeus seed extract, tocopherol acetate (vitamin E acetate), vaccinium angustifolium (blueberry) extract, vaccinium macrocarpon (cranberry) fruit extract, vitis vinifera (grape) seed extra, water

Other Information

Store below 110 oF (43 o), Read the Safety Data Sheet for this Product. You may obtain an SDS from our website: www.coretexproducts.com or Call: 1-877-684-5774

Package Label

INGREDIENTS AND APPEARANCE

CORETEX ANTIBACTERIAL HAND SANITIZER 
sd alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65753-200
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62.5 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CANNABIS SATIVA SEED (UNII: QE567Z26NG)
FRAGARIA VESCA FRUIT (UNII: CG6IX3GCMU)
PUNICA GRANATUM WHOLE (UNII: O2ZTS50U5E)
VITIS VINIFERA SEED (UNII: C34U15ICXA)
CITRULLUS COLOCYNTHIS FRUIT (UNII: 0E49E3V9U6)
EUTERPE OLERACEA WHOLE (UNII: Y57H6218HP)
GLYCERIN (UNII: PDC6A3C0OX)
HELIANTHUS ANNUUS SEEDCAKE (UNII: 482WYF7XLC)
HIPPOPHAE RHAMNOIDES FRUIT JUICE (UNII: UC3P08EB3Y)
LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
MYRCIARIA DUBIA FRUIT (UNII: YSW4EM1EKP)
PROPYLENE GLYCOL 1-BUTYRATE (UNII: PUV901J64H)
RUBUS IDAEUS SEED (UNII: M3CL7US2ZG)
VACCINIUM ANGUSTIFOLIUM WHOLE (UNII: R3538BZ1BW)
VACCINIUM MACROCARPON WHOLE (UNII: D11KO7O2DX)
WATER (UNII: 059QF0KO0R)
ACTINIDIA CHINENSIS WHOLE (UNII: 8HTD3WU8LH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
BRASSICA OLERACEA VAR. ITALICA WHOLE (UNII: DW4954EP53)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
1,3-PROPANEDIOL BIS(4-AMINOBENZOATE) (UNII: 8860R9ORQR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65753-200-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2019
2	NDC: 65753-200-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2019
3	NDC: 65753-200-03	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2019
4	NDC: 65753-200-32	44 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2019
5	NDC: 65753-200-28	118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/26/2019
6	NDC: 65753-200-05	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2019
7	NDC: 65753-200-29	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/26/2019
8	NDC: 65753-200-06	354 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2019
9	NDC: 65753-200-07	354 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/26/2019
10	NDC: 65753-200-30	473 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/26/2019
11	NDC: 65753-200-08	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2019
12	NDC: 65753-200-10	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/26/2019
13	NDC: 65753-200-20	25 in 1 CONTAINER	11/25/2019
13		3.5 mL in 1 POUCH; Type 0: Not a Combination Product
14	NDC: 65753-200-21	300 in 1 CONTAINER	11/25/2019
14		3.5 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/25/2019

Labeler - CoreTex Products (061944620)

Establishment
Name	Address	ID/FEI	Business Operations
CoreTex Products		061944620	label(65753-200)

Establishment
Name	Address	ID/FEI	Business Operations
HealthSpecialty		794053863	manufacture(65753-200)