Sweet Shimmer SWEET POMEGRANATE Hand Sanitizer

Sweet Shimmer SWEET POMEGRANATE Hand Sanitizer by

Drug Labeling and Warnings

Sweet Shimmer SWEET POMEGRANATE Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by BASE4 Ventures, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SWEET SHIMMER SWEET POMEGRANATE HAND SANITIZER- alcohol gel 
BASE4 Ventures, Inc

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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Sweet Shimmer SWEET POMEGRANATE Hand Sanitizer

Drug Facts

Active ingredient

Alcohol Denat.66%

Purpose

Antiseptic

Use

• For handwashing  to decrease bacteria on the skin

Warnings

For external use only. Flammable. Keep away from fire & flame.
Does not contain grain alcohol; do not drink. If taken internally will produce severe gastric disturbances.

When using this product

• Avoid contact with eyes and mucous membranes
• In the case of eyes or mucous membrane contact, rinse area thoroughly with water.

Stop use and ask a doctor if

• Condition worsens
• Redness or irritation develops
• Condition persists for more than 3 days

Keep out of reach of children.

If swallowed contact a doctor or Poison Control Center immediately.

Directions

• Rub dime sized amount between hands until dry.
• Supervise children in the use of this product. 
• In the case of eye contact rinse eyes thoroughly with water

Other information

• Store below 105°F
• May discolor some fabrics

Inactive ingredients

Water, Acrylate/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance, FD&C Red No. 4, D&C Red No. 33.

Questions?

Call 1-888-988-2427

Package Labeling:

SWEET SHIMMER SWEET POMEGRANATE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62651-056
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	66 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62651-056-01	29.57 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2020	04/12/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/15/2020	04/12/2021

Labeler - BASE4 Ventures, Inc (137316126)

Revised: 5/2021

Document Id: c18301c4-e123-543b-e053-2a95a90ac13e

34390-5

Set id: bd087d25-0da9-e76a-e053-2995a90a4849

Version: 2

Effective Time: 20210504