NDC 73006-350 Only For First Aid Medicine

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73006-350
Proprietary Name:
Only For First Aid Medicine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
73006
Start Marketing Date: [9]
11-15-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329 - DARK GREEN - WHITE)
PINK (C48328)
BLUE (C48333 - LIGHT BLUE)
WHITE (C48325)
Shape:
ROUND (C48348)
OVAL (C48345)
CAPSULE (C48336)
Size(s):
13 MM
11 MM
18 MM
17 MM
Imprint(s):
S77
DP
AD01
S500
Score:
1

Code Structure Chart

Product Details

What is NDC 73006-350?

The NDC code 73006-350 is assigned by the FDA to the product Only For First Aid Medicine which is product labeled by O4 Global Trading Usa, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73006-350-98 1 kit in 1 box * 1 bottle, plastic in 1 carton (73006-132-95) / 25 tablet in 1 bottle, plastic * 1 bottle, plastic in 1 carton (73006-148-95) / 25 tablet in 1 bottle, plastic * 1 bottle, plastic in 1 carton (73006-120-95) / 25 tablet in 1 bottle, plastic * 1 bottle, plastic in 1 carton (73006-143-95) / 25 tablet in 1 bottle, plastic. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Only For First Aid Medicine?

• do not use more than directed• drink a full glass of water with each dose• adults and children 12 years and over: take 2 geltabs every 6 hours; not more than 8 geltabs in 24 hours• children under 12 years: ask a doctor • take every 4 to 6 hours, or as directed by doctor• do not take more than 6 doses in 24 hours adults and children 12 years and over• take 1 to 2 caplets children 6 to under 12 years • take 1 caplet • take with a full glass of water• Do not take more than directed. SEE OVERDOSE WARNING.• do not take more than 2 caplets in 24 hoursadults and children 12 years of age and over• take 2 caplets at bedtime• do not take more than 2 caplets of this product in 24 hourschildren under 12 years of age• do not use Do not take more than directed. SEE OVERDOSE WARNING. adults and children 12 years of age and over• take 2 caplets every 6 hours while symptoms last• do not take more than 6 caplets in 24 hours, unless directed by doctor• do not take more than 10 days, unless directed by a doctor children under 12 years of age• ask a doctor

Which are Only For First Aid Medicine UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Only For First Aid Medicine Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Only For First Aid Medicine?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1049630 - diphenhydrAMINE HCl 25 MG Oral Tablet
  • RxCUI: 1049630 - diphenhydramine hydrochloride 25 MG Oral Tablet
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral Tablet
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet
  • RxCUI: 1092189 - APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".