HIMARK- alcohol liquid 
Apollo Health and Beauty Care

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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63148-403, HiMark Hand Sanitizer

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

For personal hand hygiene to help prevent the spread of bacteria, and can be used in place of hand washing if soap and water are not available.

Warnings

For external use only.

Do not use

  • On infants less than 2 months of age.
  • On open skin wounds
  • On broken or damaged skin.

When using this product

  • Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
  • Do not inhale.

Stop use and ask a doctor

if irritation or redness develops and lasts.

Keep out of reach of children

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

Other Information.

Inactive Ingredients

Water (Aqua), PEG-6, AMP-Acrylates/vinyl Isodecanoate Crosspolymer, Fragrance (Parfum), Glycerin, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Isopropyl Alcohol, Isopropyl Myristate.

Questions?

1-866-795-8481

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Package Label- 1G

HIMARK 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63148-403
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63148-403-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2023
2NDC:63148-403-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2023
3NDC:63148-403-803785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/01/2023
Labeler - Apollo Health and Beauty Care (201901209)
Registrant - Apollo Health and Beauty Care (201901209)
Establishment
NameAddressID/FEIBusiness Operations
Apollo Health and Beauty Care201901209manufacture(63148-403)

Revised: 6/2023
Document Id: fee30fb8-76f7-331c-e053-6394a90a1ca7
Set id: f9658a02-e3fa-096a-e053-6294a90afb21
Version: 2
Effective Time: 20230624
 
Apollo Health and Beauty Care