ZIMS ADVANCED ACEMANNAN AND ARNICA- allantoin gel 
NATURAL ESSENTIALS, 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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DRUG FACTS

ACTIVE INGREDIENT:

Allantoin .55%

PURPOSE:

Skin Protectant

USES:

Temporarily protects minor:

  • Cuts
  • Scrapes
  • Burns
  • Other uses of this product should be only under the advice and supervision of a doctor.

WARNINGS:

For external use only.

Do not use on:

  • deep puncture wounds
  • serious burns
  • animal bites
  • Consult a doctor for the treatment of diaper rash.

When using this product

  • avoid contact with the eyes

Stop use and ask a doctor if:

  • condition worsens, symptoms persist for more than 7 days
  • clears up and occurs again within a few days
  • under 2 years of age
  • pregnant - breast feeding

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

  • Clean hands
  • Clean site
  • Apply Zim's
  • May be covered with gauze
  • Can be used 2 to 3 times a day
  • Store at 20-25 degrees C / 68-77 degrees F.

INACTIVE INGREDIENTS:

Acemannan, Arnica, Carbomer, Methylparaben, Panthenol, Propylene Glycol, Purified Water, Trisapropylamine

Principal Display Panel - Tube Label

NEW!
ZIM'S®
ADVANCED
GEL
ACEMANNAN
Nature's Purest Form
of Aloe Vera and
ARNICA

CUTS

SCRAPES

ABRASIONS

BURNS

DEVELOPED BY A PHARMACIST

Net Wt 3 oz (85g)

Principal Display Panel - Tube Label
ZIMS ADVANCED ACEMANNAN AND ARNICA 
allantoin gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66902-800
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN5.5 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
ACEMANNAN (UNII: UZ29E6L2X8)  
ARNICA MONTANA (UNII: O80TY208ZW)  
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
WATER (UNII: 059QF0KO0R)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PANTHENOL (UNII: WV9CM0O67Z)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TRIISOPROPANOLAMINE (UNII: W9EN9DLM98)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66902-800-030.0004675 L in 1 TUBE; Type 0: Not a Combination Product01/01/201412/31/2019
2NDC:66902-800-040.0004675 L in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product01/01/201412/31/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34701/01/201412/31/2019
Labeler - NATURAL ESSENTIALS, INC. (947484713)

Revised: 3/2014
Document Id: 79fef21c-60a7-4f4a-9dda-7d048ae6c5f8
Set id: 122273ec-d670-4606-baf8-c9fe3fddebed
Version: 4
Effective Time: 20140327
 
NATURAL ESSENTIALS, INC.