- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
■ Clean affected areas with soap and warm water and dry thoroughly. ■ Apply a thin layer of Fungi-Nail® Anti-Fungal Ointment over affected area twice daily (morning and night) or as directed by a doctor. ■ Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. ■ For athlete’s foot pay special attention to spaces between the toes. ■ For athlete’s foot and ringworm, use daily for 4 weeks. ■ To prevent athlete's foot, apply once or twice daily (morning and/or night). ■ For toe fungus, apply under nail and around cuticle area. If condition persists longer, consult a doctor. ■ This product is not effective on the scalp or nails. ■ Supervise children in the use of this product.
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
-
PRINCIPAL DISPLAY PANEL
MAXIMUM STRENGTH
FUNGI-NAIL®
ANTI-FUNGAL
OINTMENT
with brush applicator
CLINICALLY PROVEN TO
CURE AND PREVENT
FUNGAL INFECTIONS
TRIPLE ACTION FORMULA
✓ Kills Fungus
✓ Stops Itching & Burning
✓ Restores Skin Health
CLINICALLY PROVEN INGREDIENT
0.7 FL. OZ. (20 g)
Convenient and Easy to Apply
Deep Penetrating Medicine that Stays in Place
Not actual size.
Patent pending.
#1 Pharmacist Recommended
FUNGI-NAIL® ANTI-FUNGAL OINTMENT
infused with 5 natural oils including tea tree, eucalyptol, aloe, olive, and lavender
For best results treat around all toenails and in between toes.
Not for Nail or scalp fungus.
Cures most athlete's foot.
For more information about Fungi-Nail® and money back guarantee, visit us at funginail.com
Kramer Laboratories, Inc.
Bridgewater, NJ 08807
kramerlabs.com
funginail.com
1-800-824-4894
K1119MAXIMUM STRENGTH
FUNGI-NAIL®
ANTI-FUNGAL
OINTMENT
KILLS FUNGUS • RESTORES SKIN
NET WT 0.7 FL. OZ. (20 G)
Distributed By:
KRAMER LABORATORIES
Kramer Laboratories, Inc. Bridgewater, NJ 08807 U.S.A.
kramerlabs.com
fungi-nail.com
1-800-824-4894
K0119 -
INGREDIENTS AND APPEARANCE
FUNGI NAIL TOE AND FOOT
tolnaftate ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55505-185 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Tolnaftate (UNII: 06KB629TKV) (Tolnaftate - UNII:06KB629TKV) Tolnaftate 1 g in 100 g Inactive Ingredients Ingredient Name Strength Aloe Vera Leaf (UNII: ZY81Z83H0X) Carbomer Homopolymer Type A (Allyl Pentaerythritol Crosslinked) (UNII: F68VH75CJC) Dimethicone 350 (UNII: 2Y53S6ATLU) Eucalyptol (UNII: RV6J6604TK) Lavender Oil (UNII: ZBP1YXW0H8) Glyceryl Monostearate (UNII: 230OU9XXE4) Olive Oil (UNII: 6UYK2W1W1E) Phenoxyethanol (UNII: HIE492ZZ3T) Poloxamer 188 (UNII: LQA7B6G8JG) Water (UNII: 059QF0KO0R) Sodium Hydroxide (UNII: 55X04QC32I) Tea Tree Oil (UNII: VIF565UC2G) Product Characteristics Color WHITE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55505-185-50 1 in 1 CARTON 06/01/2019 1 20 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 11/15/2018 Labeler - Kramer Laboratories (122720675) Establishment Name Address ID/FEI Business Operations Denison Pharmaceuticals, LLC 001207208 manufacture(55505-185)