EVERY MAN JACK - HAND SANITIZER 62 PERCENT- ethyl alcohol gel
EVERY MAN JACK

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.

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EVERY MAN JACK - HAND SANITIZER GEL (62% ETHANOL) - 57934-5014

ACTIVE INGREDIENT

ETHYL ALCOHOL 62%

PURPOSE

ANTISEPTIC

USES

FOR HAND WASHING TO DECREASE BACTERIA ON SKIN.

WARNINGS

FOR EXTERNAL USE ONLY.

FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.

DO NOT USE IN EYES. IF CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER. STOP USE AND ASK A DOCTOR IF REDNESS AND IRRITATION DEVELOP AND 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 AIR DRY.

OTHER INFORMATION

STORE AT ROOM TEMPERATURE. MAY DISCOLOR CERTAIN FABRICS.

INACTIVE INGREDIENTS

CITRUS: PURIFIED WATER, GLYCERIN, CARBOMER, TRIETHANOLAMINE, TOCOPHERYL ACETATE, COCONUT OIL, CITRUS MEDICA (LEMON) PEEL OIL, ALOE VERA, FRAGRANCE

SEA SALT: AQUA/WATER, GLYCERIN, CARBOMER, CITRUS MEDICA LIMONUM (LEMON) PEEL OIL, TRIETHANOLAMINE, TOCOPHERYL ACETATE, COCUS NUCIFERA (COCONUT) OIL, ALOE BARBADENSIS (ALOE) LEAF JUICE, FRAGRANCE

01b LBL_EMJ_hand-sanitizer-citrus-6.7oz-00079-v2

01b LBL_EMJ_Hand Sanitizer Gel_Sea Salt_236mL_US

EVERY MAN JACK - HAND SANITIZER 62 PERCENT
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:57934-5014
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
COCONUT OIL (UNII: Q9L0O73W7L)
LEMON OIL (UNII: I9GRO824LL)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:57934-5014-5	150 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
2	NDC:57934-5014-6	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
3	NDC:57934-5014-2	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
4	NDC:57934-5014-3	73 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020
5	NDC:57934-5014-1	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/04/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	05/04/2020

Labeler - EVERY MAN JACK (013586921)