Search by Drug Name or NDC
NDC 69626-0049-04 TANAC Oral Pain Reliever 10 g/100mL Details
TANAC Oral Pain Reliever 10 g/100mL
TANAC Oral Pain Reliever is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Leosons Overseas Corp. The primary component is BENZOCAINE.
Product Information
NDC | 69626-0049 |
---|---|
Product ID | 69626-0049_b6fdb7e4-7bc5-8297-e053-2a95a90a4379 |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | TANAC Oral Pain Reliever |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Benzocaine |
Product Type | HUMAN OTC DRUG |
Dosage Form | LIQUID |
Route | ORAL |
Active Ingredient Strength | 10 |
Active Ingredient Units | g/100mL |
Substance Name | BENZOCAINE |
Labeler Name | Leosons Overseas Corp |
Pharmaceutical Class | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH NOT FINAL |
Application Number | part356 |
Listing Certified Through | 2023-12-31 |
Package
Package Images

NDC 69626-0049-04 (69626004904)
NDC Package Code | 69626-0049-4 |
---|---|
Billing NDC | 69626004904 |
Package | 1 BOTTLE in 1 CARTON (69626-0049-4) / 13.3 mL in 1 BOTTLE |
Marketing Start Date | 2015-01-01 |
NDC Exclude Flag | N |
Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 81cc61fa-31a7-2214-e053-2a91aa0ae46a Details
Active Ingredients & Purposes
Uses
Warnings
For oral use only.
Methemoglobinemia warning: Use of this product may cause methemoglobinemia, a serious
condition that must be treated promptly because it reduces the amount of oxygen carried in
blood. This can occur even if you have used this product before. Stop use and seek immediate
medical attention if you or a child in your care develops:
- pale, gray, or blue colored skin (cyanosis)
- headache
- rapid heart rate
- shortness of breath
- dizziness or lightheadedness
- fatigue or lack of energy
Allergy alert: do not use this product if you have a history of allergy to local anesthetics such as
procaine, butacaine, benzocaine, or other “caine” anesthetics. If a skin reaction occurs, stop use
and seek medical help right away.
Stop use and ask a doctor or dentist if
- sore mouth symptoms do not improve in 7 days
- symptoms clear up and occur again within a few days
- irritation, pain or redness persists or worsens swelling, rash, or fever develops
Directions
Other information
Inactive ingredients
Questions?
Principal Display Panel
INGREDIENTS AND APPEARANCE
TANAC ORAL PAIN RELIEVER
benzocaine liquid |
||||||||||||||||||||
|
||||||||||||||||||||
|
||||||||||||||||||||
|
||||||||||||||||||||
|
||||||||||||||||||||
|
Labeler - Leosons Overseas Corp (148605470) |