MOLECULAR AF- tolnaftate oil

Molecular AF by

Drug Labeling and Warnings

Molecular AF by is a Otc medication manufactured, distributed, or labeled by Renu Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Tolnaftate 1%

For External use only

Do not use on children under 2 years of age unless directed by a doctor

When using this product avoid contact with the eyes

Stop use and ask a doctor if

• irritation occurs
  
• there is no improvement within 4 weeks

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away

Directions:

• clean the affected area and dry thoroughly
• apply a thin layer over the affected area twice daily
  (morning and night)
• supervise children in the use of this product
• for athlete’s foot, pay special attention to the spaces
  between toes. Wear well-fitting, ventilated shoes, and
  change shoes and socks at least once daily
• use daily for 4 weeks. If condition lasts longer, ask
  a doctor
• to prevent athlete’s foot, apply to the feet once
  or twice daily
• this product is not effective on the scalp or nails
  

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MOLECULAR AF 
tolnaftate oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76348-401
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV)	TOLNAFTATE	0.01 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
CINNAMON OIL (UNII: E5GY4I6YCZ)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
OLIVE OIL (UNII: 6UYK2W1W1E)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
TEA TREE OIL (UNII: VIF565UC2G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76348-401-01	11.5 mL in 1 BOTTLE
2	NDC: 76348-401-02	11.5 mL in 1 BOX

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333C	07/01/2011

Labeler - Renu Laboratories, Inc. (945739449)